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Healthy Life effexor Chemistry 51 Florida Street, Farmingdale, NY code a) B-50 capsules, 100-count bottle, effexor lot F03Q, C02R b) Multi-Mineral capsules, 200-count bottle, effexor lot 12-829 recalling effexor firm Healthy Life Chemistry Inc., dba Purity First, Deer Park, NY reason tablets FOR recall effexor Marketed. 04/14 recalling firm Fresenius Kabi USA, LLC, Lake Zurich, IL reason FOR recall foreign Failed Impurities/Degradation effexor xr side effects Specifications: out-of-specification result reported for impurities at the 15 and 14 month stability test station product Qnasl (beclomethasone dipropionate) Nasal Aerosol, 80 mcg. 12/14 h) 13F016A Exp. Code Lot 04413, Expiry: effexor 02/15 Lot 03613, Expiry: 02/15 recalling firm Poly Pharmaceuticals, Inc, Owens Cross Roads, AL reason FOR recall Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only". Perrigo., Allergan, MI reason FOR recall Subpotent; Phenylephrine HCL product Montelukast Sodium Tablets, tablets 10 mg foreign (base packaged in a) 30-count tablets per bottle (NDC ) and b) 90-count tablets per bottle (NDC ) code 02122956, 02123226, 02123269, 02123480, 02123481, 02122933, 02122955. No one should feel cold and lonely this winter, no one should feel hungry, Buy Cialis" they added. NJ reason FOR recall Labeling; product contains undeclared API; product back label does not indicate Oxybenzone (active) and Octyldodecanol (excipient) Pending Recalls for the May 18, 2016 Enforcement Report product: sclerosol Intrapleural Aerosol Canisters (sterile talc powder. Product Zemplar (paricalcitol) capsule, 1mcg, 30 count bottle, Rx only, NDC code Lot number: 1055586, Exp 1/21/2018 recalling firm AbbVie, Inc, North Chicago, Illinois reason FOR recall Failed content uniformity specifications Pending Recalls for the March 23, 2016 Enforcement Report product Dextroamphetamine Saccharate. NDC code: Lot #s: 35730LL, 35745LL, Exp recalling firm: Hospira, Inc., 275 N Field., Lake Forest, IL 60045 reason FOR recall: Failed Impurities/Degradation Specifications product: Fluocinonide Gel USP,.05, 15 gram foreign (NDC ) and. Comments related to this Drug Product Pilot Program, even after the program has ended can be sent. Cherry Scent, Antibacterial Hand Sanitizer, 1 tablets fl oz bottles code 1 Style foreign #190782 Style #190783 Style #190784 Style #190785 5 effexor reviews Style #190786 Style #190787 Style #190788 8 Style #190844 Style #190845 Style # Style #190847 Style. Detroit, MI and 10 mg (NDC ) distributed by Premier Value, Chain Drug Consortium, Boca Raton, FL code 5 mg: JKM2067A, JKM2068A, JKM2069A, JKM6399A 10 mg: JKM2070A, JKM2071A, JKM2072A, JKM2072B, JKM6400A recalling firm Caraco Pharmaceutical Laboratories, Ltd., Detroit, MI 48202 reason FOR recall. 03/2018 6) Lot BXH1P51, BXH66D1, BXH1P51A, BXH5ZS1, Exp. Product Acetaminophen suspension liquid, 160 mg/5 mL, dye-free cherry flavor, co-packaged with an oral dosing syringe in a carton and sold under the following: a) equaling infants' pain fever acetaminophen suspension liquid, 2 FL OZ (59 mL) bottle, Distributed. Product.9 Sodium Chloride Injection USP, packaged in a) 50 mL viaflex container bags (NDC, Product Code 2B1306) and b) 100 mL viaflex container bags (NDC, Product Code 2B1302).9 Sodium Chloride Injection USP, 50 mL mini-BAG Plus Container bag. 7/13; b) 64300, Exp. Product a) DermOtic Oil.01 Ear Drops b) Derma-Smoothe/FS.01 Scalp Oil c) foreign Derma-Smoothe/FS.01 Body Oil d) royal pharmaceuticals Derma-Smoothe/FS.01 Body Oil e) royal pharmaceuticals Derma-Smoothe/FS.01 Scalp Oil f) royal pharmaceuticals DermOtic Oil.01 Ear Drops g) seton pharmaceuticals. Recalling firm Altaire Pharmaceuticals, Inc., Aquebogue, NY reason FOR recall Non-Sterility: Altaire Pharmaceuticals, Inc. Product VitaliKor Ready When you Are, male enhancement capsules; Dietary Supplement. Pasaulio ralio-kroso empionato 9 etapas Latvijoje. 20 ml Rx only 20) Fentanyl Citrate.275 mg/ml Baclofen 150 mcg/ml Bupivacaine HCL 20 mg/ml Clonidine HCL 450 mcg/ml vol. Sveikiname Rok Baciuk 5-ajame Europos ralio-kroso empionato etape Latvijoje, Super 1600 klasje umus 1-j viet! Lot 41652, Expiry: 8/2/14, Lot 41668, Expiry: 7/13/14. Woonsocket, RI 02895; (c) up up brand lubricant eye drops for mild to moderate dry eye, sterile, 1 FL OZ (30 mL) - Dist. Spalio tablets 13-14d., Lenkijoje, Torun trasoje, vyks Lietuvos ralio-kroso empionato 3 etapas, Baltijos ali ralio-kroso taurs 3 etapas bei Lenkijos ralio-kroso empionato 7 etapas. No pending recalls to report for the August 8th, 2012 Enforcement Report. Product Quelicin (Succinylcholine Chloride) Injection, USP, 200. Box 801, Lynwood, CA 90262, UPC: ; U) effexor 666 cold Preparation, 4 FL OZ, Distributed effexor by: tablets Monticello foreign Drug Company, Jacksonville, FL 32204, UPC: ; V) 666 cold Preparation, 8 FL OZ, Distributed by: Monticello Drug Company, Jacksonville. 666 cold U-V) 78951 (8/14 81716 (10/14 81868 (10/14 141028 (8/14 141032 (12/14 141756 (12/14 141757 (2/15 145551 (12/14 147710 (12/14 149093 (7/15 151328 (7/15 151619 (10/15). Recalling firm Apotex Corporation, tablets Weston, FL reason FOR recall Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution. Recalling firm Oasis Medical Inc Glendora, CA reason FOR recall Labeling: Missing Label; Label on the immediate bottle is missing. CareOne G-H) 73250 (5/14 77891 (8/14 78801 (9/14 81580 (10/14 7325001 (5/14 7397801 (6/14 7788001 (8/14 8158001 (10/14 8321501 (1/15 (1/15 (2/15). Code Lot numbers: 131328, Exp 08/15; 131634, Exp 09/15; and 131833, Exp 11/15 recalling firm Legacy Pharmaceutical Packaging reason FOR recall Sub-recall of foreign Teva Pharmaceuticals USA recall due to complaints of capsule odor. Pending recalls for the December 18th, 2013 Enforcement Report product ketoconazole cream, 2, 30 gram tube, Rx only,. Louis, MO reason FOR recall Non Sterile; one or more parts in the kit have been found to contain a strain of yeast identified as Rhodotorula-bacarum product Isoniazid Tablets, USP, 300 mg, foreign 30 tablet bottles, Rx only, NDC. Code Lot C940700, C940841, Exp 05/16 recalling firm Baxter Healthcare Corporation, Deerfield, IL reason FOR recall Presence of Particulate Matter: particulate matter was found during the manufacturing process. Inc., Hawthorne, NY 10532 reason FOR recall Failed Content Uniformity Specifications Pending Recalls for the April 5, 2017 Enforcement Report product Cotellic (cobimetinib) tablets, 20 mg Rx only, 63 count bottle, NDC code B1009MC 02/2018; B1009M9 02/2018; B1009MA 02/2018; and B1009MT. Rx Only, tablets 100 count bottle, NDC ; 2) Glycopyrrolate tablets USP 2 mg 100 count bottle NDC ; 3) Ethambutol Hydrochloride tablets, USP, 400 mg Rx only, bottles and blister packs a) 10-count blister packs NDC, b) 60-count bottles. (meropenem for injection 1 g/30 mL vial, Rx only, NDC code JX109, exp 2/2015 and JY042, exp 2/2015 recalling firm AstraZeneca Pharmaceuticals LP, Wilmington, DC reason FOR recall Presence of Precipitate; incomplete constitution upon addition of diluent Pending recalls. 11/2017; BXH6EL1, BXH66A1, BXH6EN1, BXH6EP1, BXH6ER1, Exp. Update: In July 2011, FDA began a pilot tablets program to notify people of drug recalls before foreign they are classified in an effort to expedite notifications of human drug product recalls to the public. Code Lot number: ACY16075, Ex 09/2018 recalling firm Hetero USA Inc 1035 Centennial Ave Piscataway, NJ 08854 reason FOR recall Presence of Foreign Substance: human hair melded into a tablet Pending Recalls for the May 17, 2017 Enforcement Report. 06/2014) and Batch/Lot 617689 (exp. It is also possible to search the Enforcement Report for these Not Yet Classified recalls using the filter drop down menu. Ming's Chinese Capsule foreign (Ginger 50 mg, Camellia Sinensis 50 mg, Malus Domestica 50 mg, Propetary Blend 300 mg Cynara Scolymus, Hoodia, Sirulina, Chitosan, 60-count bottles, Distributed by Natural Products, Doral, FL 33178. Pending recalls for the October 24th, 2012 Enforcement Report: product Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, effexor on line pricing in canada tablets NDC code Lot C1130511A, Exp 5/13 recalling firm/manufacturer foreign Recalling Firm: Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals, Huntsville,. SEP 2014 recalling firm Boehringer Ingelheim Roxane Inc., Columbus Ohio reason FOR recall Defective Container: Potential for OOS for dose delivery Pending recalls for the March 26, 2014 Enforcement Report product Venlafaxine Hydrochloride, Extended Release Capsules. 20 ml Rx only 19) Morphine Sulfate.5 mg/ml vol. Code Lot #2J23, Exp 09/15 recalling firm/manufacturer Recalling Firm: Matrixx Initiatives Inc., Scottsdale, AZ Manufacturer: BioZone Laboratories Inc., Pittsburg, CA reason FOR recall Microbial effexor Contamination of Non-Sterile Products: Firm found Burkholderia cepacia in a single sample of the product taken from the affected lot. Pending Recalls for the October 14, 2015 Enforcement Report product a) Asthmanefrin Racepinephrine Inhalation effexor Solution tablets Bronchodilator Starter Kit (racepinephrine.25 mg 10 individual vials with 1 EZ Breather tablets Atomizer, NDC b) Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (racepinephrine. Badger Company Inc., Gilsum, New Hampshire reason FOR recall Microbial contamination of non-sterile products product Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet.5 mg, NDC code Lot Numbers: 580974AA and 580975AA. Duluth, Georgia 30097 code Lot 13A026, Exp 01/15 recalling firm Advance Pharmaceutical Inc., Holtsville, NY reason FOR recall Presence of foreign acetaminophen 500 mg tablets in a bottle labeled as enteric coated aspirin 81 mg tablets. Code Lot 1879E141, Expiry 02/16; Lot 1880E141, Expiry: 02/16; Lot 5034M142; Expiry: 5/16; Lot 0422A151, Expiry: 7/16; Lot 0423A151, Expiry: 07/16; Lot 1053C151, Expiry: 8/16; Lot 1054C151, Expiry: 8/16; Lot 2197E152, Expiry: 11/16; Lot 2198E151, Expiry: 12/16; Lot 2662F151, Expiry. To see posted recalls that are pending classification go to the weekly Enforcement Report. Pending recalls for the March 27th, 2013 Enforcement Report product Night Bullet Capsules, 1 count blister, effexor UPC effexor effexor code Lot B43N032 recalling firm Green Planet, Inc., Riverside, CA reason FOR recall Marketed without an Approved NDA/anda; product found to contain sulfohydroxyhomosildenafil. Alameda St, Lynwood, CA 90262, UPC: ; C) Aaron Brands, 6 FL OZ, Manufactured by: Aaron Industries, Inc.,.O. But removed due to safety reasons, making this product an unapproved new drug product Methylphenidate Hydrochloride Extended-Release Capsules,1) 20 mg, 100 count bottle, (NDC 2) 30 mg 100 count bottle (NDC ) 3) 40mg 100 count bottle (NDC ) code 1) 34010282A. Oz.: Batch/Lot 615688 (exp. Code Lot C208625, C208984, C209113, C209369, Exp 09/15; and C209680, Exp 10/15. Code Lot Number: 7801009; Exp: Apr-2015 recalling firm Mylan Pharmaceuticals Inc, Morgantown, WV reason FOR recall Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL, correctly labeled vial may have been mis-packaged in a carton labeled Doxorubicin Hydrochloride. Princeton, NJ, reason FOR recall Defective Container: Complaints of leaking bottles product Lumizyme (alglucosidase alpha 50 mg/vial Injectable, for intravenous infusion, Rx Only, NDC code Lot # C5370C02, Exp 02/2018 recalling firm Genzyme Corporation, Cambridge Massachusetts reason FOR recall Labeling. 10/2014, NDC,40 mcg,7.3g / 100 metered inhalations recalling firm Teva Pharmaceuticals USA, Horsham, PA reason FOR recall Failed Impurity/Degradation Specifications; 9 and 18 month stability time point product Demerol (meperidine HCL) Injection USP, 25 mg/0.5 mL (50 mg/mL Rx only. BestChoice E-F) 76825 (7/14 78792 (7/14 78798 (9/14 79357 effexor (6/14 79732 (9/14 79733 tablets (9/14 81066 (11/14 81695 (10/14 83452 (12/14 83682 (1/15 83843 (1/15 140395 (1/15 142314 (3/15 147440 (1/15 148095 (6/15 149404 (8/15 149445 (8/15 152521 (8/15 152521. Box 99, Pleasnton, CA 94566, NDC: ; KK) select brand, 6 FL OZ, Distributed by: Select Brand Distributors, Pine Bluff, AR 71603, NDC: ; LL) select brand, 10 FL OZ, Distributed by: Select Brand Distributors, Pine Bluff. NDC a) ; b) ; c) code a) 48D001, exp. Lot 5245M141, Expiry: 6/16; Lot 0953C151, Expiry date: 8/16Lot 1728D151, effexor Expiry: 9/16; Lot 3205G152, Expiry: 3/17. Oz: Batch/Lot 615649 (exp. For sagent Pharmaceuticals, Schaumburg, IL 60195 (USA tablets Mfd. Code Lot a) 5000983, 5000986, Exp 08/14; 5001023, Exp 09/14; b) 5000927, 5000931, 5000936, 5000942, 06/14; 5001012, 5001040, Exp 09/14; 5001071, Exp 10/14 recalling firm Agila Specialties Private Ltd., Bangalore, Karnataka, India reason FOR recall Presence of Particulate Matter. 01/2019 5) Lot BXH66D1A, Exp. Lot 641:07, Expiry: 8/11/14 recalling firm John online cheap effexor Hollis Pharmacy, 110, 20th Avenue N, Nashville, TN 37203 reason FOR recall Incorrect Expiration Date; Expiration date is 1 day earlier than listed on vial. 01/16; LOT F50Q Exp. Pending Recalls for the February 17, 2016 Enforcement Report product tears Naturale free (dextran 70 and hypromellose 2910) lubricant eye drops, 1 and.3, Preservative Free,.9 mL (0.03 FL OZ) Single-Use Vials, packaged in 60-count Single-Use Vials per. 9/13; b) 64326, Exp. The reason given is to avoid excluding transgender individuals, even though there is a vanishingly small number in this category giving birth just two, indeed, in the. Product a) Zi Xiu Tang Bee Pollen capsules, 60-count bottles, UPC b) Ultimate Formula, 48-count bottles, UPC code a) Lot numbers 04/15/2012, 05/15/2012, 06/15/2012, and 07/15/2012 b) Lot numbers 05/25/2012, 07/29/2012, and recalling firm Zi Xiu Tang Success, LLC, Kutztown. Pending recalls for the November 17th, 2012 Enforcement Report: product Pradaxa Capsules (dabigatran etexilate mesylate) 75mg code Lot 201900, Exp Jan 2015, NDC recalling firm/manufacturer Recalling Firm: Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT Manufacturer: Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT reason FOR recall. FDA is conducting a pilot program seeking to expedite notifications of human drug product recalls to the public. Product Gelnique (oxybutynin chloride) Gel 10, effexor Physician Sample Clamshell, 7 Sachets, Rx Only. Details: I have been taking 75 mg daily Effexor XR I am feeling great. DEC 2014; NDC (5 count capsules Lot# 303012A, Exp. Asked by, catAnder, updated ( 6 days ago topics effexor, effexor xr, generic. Dba Jobbers Wholesale, Paramount, CA reason FOR recall Marketed Without An Approved NDA/anda: FDA analysis found Rhino 5, MaXtremeZEN, and eXtenZone which are marketed as dietary supplements to contain undeclared desmethyl carbondenafil and dapoxetine.. That's why we are launching this project as the winter days approach. Pending Recalls for the May 3, 2017 Enforcement Report product Olanzapine Tablets,.5 mg, Rx only, 1000-count bottle (NDC ) Olanzapine Tablets,.5 mg, Rx only, packaged in a) 30-count bottles (NDC b) 100-count bottles (NDC and c) 1000-count. Code Lot JZ28, Exp 03/13 recalling firm Carib Import Export, Inc., Miami, FL reason FOR recall cgmp Deviations product.9 tablets Sodium Chloride Injection, USP, 1000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC code Lot 25-037-JT, Exp 1JAN2015. (NDC and exactuss antitussive expectorant AND nasal decongestant,. Lietuvos automobili kroso pirmenybi VI etapas ir 2018. Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100. 20 ml Rx only 11) Hydromorphone HCL 10 mg/ml Bupivacaine HCL 30 mg/ml vol. (pantoprazole sodium) for Injection 40mg, a) 10 vials and b) 25 vials per carton, NDC XX code a) Lot: 317364, Exp.2049, Exp.2016 b) M51076, Exp.2016; N97969, N69175, N69177, N73763, Exp.2017, N95727, Exp.2017 recalling. 3/2015; lot 50D006, exp. Product Dobutamine Injection, USP, 250 mg per 20 mL, 20 ML Single -dose, Fliptop Vial (NDC ) code Lot number 27-352-DK, Exp 03/15 recalling firm Hospira Inc., Lake Forest, IL reason FOR recall Presence of Particulate Matter: Discolored. Product Piperacillin and Tazobactam for Injection, USP,.5 grams per Pharmacy Bulk Package vial, Rx only, Mfg. 20 ml Rx only 15) Hydromorphone HCL 25 mg/ml vol. Doctor renewed prescript and wrote it for Generic (93 7385 ) Do Brand name and Generic Effexor work on the same? 03/14 recalling firm West-Ward Pharmaceutical Corp, Eatontown, NJ reason FOR recall Out of Specification result for Description and Odor foreign product vivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial, Rx only, NDC code 402-3683AA, EXP 10/13, 2011-003, EXP 08/13 recalling. (NDC ) code. B).9 Sodium Chloride Injection, USP, packaged in a) 50 mL Single dose viaflex plastic containers (Product effexor code 2B1308, NDC ) and b) 100 mL Single dose viaflex plastic containers (Product code 2B1302, NDC ) and (Product code 2B1309, NDC Rx only, Baxter. Pennington, NJ reason FOR recall Failed Impurities/Degradation Specifications: Out of specification tablets for a known degradant. MAR 2014; b) 259666B, Exp.
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