Camber pharmaceuticals recalls

    • [PDF File]Smith Drug Company

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_ae9058.html

      CAMBER PHARMACEUTICALS, INC. Manufacturing Firm: Camber Pharmaceuticals, Inc. 1031 Centennial Ave. Piscataway, NJ 08854 Product Description Famciclovir Tablets 31722-00141-01000337 Smith Drug 9098 Fair-forest rD Spartanburg, SC 29301 URGENT: Drug Recall Notice nd Date: February 2 , 2018 NDC Number Package Size Lot # I Expiration Date FMC17039

    • [PDF File]Drug Information Center Highlights of FDA Activities – 3/1 ...

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      Pharmaceutical Packaging recalled 40 repackaged lots of losartan following the recall initiated by Camber Pharmaceuticals in February. Updated information on the ARB recalls can be found on the FDA site.

    • [PDF File]Do Americans Have Access to High Quality Generics

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_26238c.html

      Pharmaceuticals Inc. •Hetero Labs, Inc. labeled as Camber Pharmaceuticals, Inc, RemedyRepack, Inc., AvKARE, Preferred Pharmaceuticals, Inc •Torrent Pharmaceuticals Limited RemedyRepack, Inc. RECALLS AND DRUG SHORTAGES •Due to this recall, there is little replacement

    • [PDF File]UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK

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      practices in China; however, over the next several months, recalls continued to expand to other overseas laboratories in India. 12. Previous recalls, such as a recall by Camber Pharmaceuticals announced on August 8, 2018, implicated specific manufacturing facilities in India as a source of contaminated valsartan medication.

    • 2020 Drug Recall DE 02.10.2020 - MMIT

      Pharmaceuticals) 60mg/10ml 25021‐0241‐10 613296 exp. 04/2020 1/24/2020 This recall is being issued due to the trending of impurity results detected during testing of stability samples for one lot. retail‐level Montelukast (Macleods Pharmaceuticals Limited)

    • Supplementary file 12: Recalls and alerts of poor quality ...

      Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Valsartan Tablets, USP, 40mg, 80mg, 160mg and 320mg Due to The Detection of Trace Amounts of N-Nitrosodimethylamine (NDMA) Impurity, Found in an Active Pharmaceutical Ingredient (API) | FD.

    • [PDF File]THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF NEW ...

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      i. Camber Pharmaceuticals, Inc. 15. Defendant Camber Pharmaceuticals, Inc. is a Delaware corporation, with its principal place of business at 1031 Centennial Avenue, Piscataway, NJ 08854.6 ii. Hetero Drugs, Ltd. 16. Defendant Hetero Drugs, Ltd. is a foreign corporation with its principle place of

    • [PDF File]CAMsE - Smith Drug Company

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      4.Notifications of this recall are being sent to all direct distributor accounts of Camber. If you further distributed this product, please forward this notification to your customer as it is a CONSUMER LEVEL RECALL. 5.Contact recall@qualanex.com to obtain response form and a pre-paid shipping label in order to return the recalled

    • [PDF File]Voluntary Recall Letter - Doctors HealthCare Plans, Inc.

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_91f224.html

      If you have any medical questions regarding this recall, please contact Camber Pharmaceuticals, Inc. at 1-866-495-1995 (8:00 am – 4:30 pm Eastern Time). Consumers with questions regarding this recall can contact your dispensing pharmacy during normal business hours.

    • [PDF File]Weekly Recall Report - Amwins Rx

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_b1726f.html

      for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-90 Lot #: E181370, Exp. 5/2020 Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg. Not Yet Classified Zoledronic Acid Injection, 5mg/100 mL (0.05 mg/mL) 100ml vial, Rx Only.

    • [PDF File]2019 Drug recalls - Blue Cross Complete

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      February 28 - Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 25 mg, 50 mg and 100 mg Due to the Detection of Trace Amounts of N-Nitroso N -Methyl 4-amino butyric acid (NMBA) Impurity found in the Active Pharmaceutical Ingredient (API).

    • [PDF File]UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_492244.html

      Previous recalls, such as the Camber Pharmaceuticals recall announced on August 8, 2018, implicated specific manufacturing facilities in India as a source of contaminated valsartan medication.

    • [PDF File]Cigna Pharmacy Management Prescription Medication Recall

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_61e6a8.html

      this notice, Camber Pharmaceuticals, Inc. hasn’t received any complaints or inform ation about medical illness or harmful effects caused by the recalled medication. As of August 31, 2018, this is the only lot number affected by this recall: Medication/Dosage/Amount Lot number It’s either on the label printed by the pharmacy

    • [PDF File]Losartan Potassium tablets

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_f61795.html

      Camber Pharmaceuticals, Inc. is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. This recall was prompted due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) a possible process impurity or contaminant in an active pharmaceutical ingredient,

    • [PDF File]Drug Recall List - BCBSM

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      NOTE: This is not a complete list of all recalls. Please see FDA.gov >Drugs>Drug Safety and Availability> Drug Recalls for additional information. 1-888-721-7115 Naproxen Sodium 06846217801 06846217901 06846217905 CGMP Deviations If you have questions about this recall, Glenmark Pharmaceuticals Inc, 1-888-721-7115 September 2021 Class II

    • [PDF File]UNITED STATES DISTRICT COURT DISTRICT OF NEW JERSEY

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_45552d.html

      Torrent sourced valsartan directly from Zhejiang Huahai Pharmaceuticals. 5. After the first wave of recalls, on August 17, 2018, Defendant Torrent’s parent company, Torrent Pharmaceuticals Limited, issued a voluntary recall of fourteen (14) lots of Valsartan/Amlodipine/HCTZ tablets “to the consumer level due to the detection of trace

    • [PDF File]Making sense of the recent blood pressure drug recalls

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_751637.html

      Last week alone, two ARB drug recalls occurred. Camber Pharmaceuticals recalled 87 lots of losartan potassium tablets last Friday because they contain N-Nitroso-N-methyl-4-aminobutyric acid

    • [PDF File]Pharmacy Recalls and Withdraws

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      and 100mg to the consumer level. This recall was prompted due to Camber Pharmaceuticals, Inc. issuing a Voluntary Nationwide Recall of Losartan Tablets, USP, due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) a possible process impurity or contaminant in an active pharmaceutical

    • [PDF File]ISSN-2230-7346 Journal of Global Trends in Pharmaceutical ...

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_60870d.html

      List of Voluntary Recalls by the companies. Sl. No. Ranitidine Valsartan 1 Denton pharma, Inc, dba northwind pharmaceuticals Prinston pharmaceuticals 2 Mylan laboratories Teva Pharmaceuticals 3 Apco pharma LLC Camber Pharmaceuticals 4 Glenmark pharmaceuticals Inc., USA ScieGen 5 Precision dose Inc, oral solution Torrent Pharmaceuticals

    • [PDF File]Legacy Pharmaceutical Packaging – Recall of losartan

      https://info.5y1.org/camber-pharmaceuticals-recalls_1_4cc168.html

      recalls (Torrent, Camber) of some lots of losartan tablets due to the detection of trace amounts of an unexpected impurity, N-Nitroso N-Methyl 4-amino butyric acid (NMBA), a possible process impurity or contaminant in an active pharmaceutical ingredient, manufactured by Hetero Labs Limited.

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