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Is Amlodipine recalled?

95 FDA recalls mention Amlodipine. The most recent are listed below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Amlodipine.

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate Tablets, USP 10 mg, packaged in a) 90-count bottles (NDC 0378-5210-77) and b) 500-count bottles (NDC…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-5210-77 D-66403-012

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 10 mg/40 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6900-01 D-66403-010

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 10mg/20mg, in 100 count bottles (NDC# 0378-6898-01) and 500 count bottles (NDC#…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6898-01 D-66403-009

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 5 mg/40 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6899-01 D-66403-008

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 5 mg/20 mg, packaged in a) 100-count bottles (NDC 0378-6897-01) and b) 500-count…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6897-01 D-66403-007

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 5 mg/10 mg, packaged in a) 100-count bottles (NDC 0378-6896-01) and b) 500-count…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6896-01 D-66403-006

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate Tablets, USP, 5 mg, packaged in a) 90-count bottles (NDC 0378-5209-77) and b) 500-count bottles (NDC…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-5209-77 D-66403-005

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate and Benazepril HCl Capsules, 2.5 mg/10 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-6895-01 D-66403-002

Class II · Moderate risk Terminated Sep 13, 2013

Amlodipine Besylate Tablets, USP, 2.5 mg, packaged in a) 90-count bottles (NDC 0378-5208-77) and b) 500-count bottles (NDC…

Reason CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

Mylan Pharmaceuticals Inc. NDC 0378-5208-77 D-66403-001

Class II · Moderate risk Terminated Aug 8, 2013

Exforge (amlodipine and valsartan, Tablets) 10/320 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9491-07 D-334-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge (amlodipine and valsartan Tablets) 10/160 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9489-07 D-333-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 5/160/25 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9560-89 D-332-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 5/160/12.5 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9559-89 D-331-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 10/320/25 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9563-89 D-330-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge (amlodipine and valsartan Tablets) 5/320 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9490-07 D-329-2014

Class II · Moderate risk Terminated Aug 8, 2013

Exforge (amlodipine and valsartan Tablets) 5/160 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured…

Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…

Novartis Pharmaceuticals Corp. NDC 0078-9488-07 D-328-2014

Class II · Moderate risk Terminated Jul 2, 2013

amLODIPine BESYLATE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093716798.

Reason Labeling: Label Mixup: amLODIPine BESYLATE, Tablet, 5 mg may have potentially been mislabeled as the following drug: CYANOCOBALAMIN, Tablet, 1000…

Aidapak Services, LLC D-843-2014

Class II · Moderate risk Terminated Jul 2, 2013

amLODIPine BESYLATE, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68382012316

Reason Labeling:Label Mixup; amLODIPine BESYLATE, Tablet, 10 mg may be potentially mislabeled as FINASTERIDE, Tablet, 5 mg, NDC 16714052201, Pedigree…

Aidapak Services, LLC D-726-2014

Class II · Moderate risk Terminated Apr 22, 2013

Walmart Amlodipine Besylate Tablets, USP 10 mg, Rx only, 30 tablets, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge…

Reason Labeling: Label Error on Declared Strength-The recalled product has a misprint on the Amoldipine 10 mg label, 5 mg is listed in the USP description…

Legacy Pharmaceutical Packaging LLC NDC 68645-445-70 D-319-2013

Class II · Moderate risk Terminated Apr 9, 2012

Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd. By: Dr. Reddy's…

Reason Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril…

Dr. Reddy's Laboratories, Inc. NDC 55111-340-05 D-1434-2012