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U.S. Department of Health and Human Services

FDA Application

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NDC Search Results on Active Ingredient: Chloroquine

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
CHLOROQUINE PHOSPHATE 37662-0273-2  Hahnemann Laboratories, INC.    HUMAN OTC DRUG  unapproved homeopathic 
CHLOROQUINE PHOSPHATE 37662-0271-1  Hahnemann Laboratories, INC.    HUMAN OTC DRUG  unapproved homeopathic 
CHLOROQUINE PHOSPHATE 37662-0266-1  Hahnemann Laboratories, INC.    HUMAN OTC DRUG  unapproved homeopathic 
CHLOROQUINE PHOSPHATE 37662-0271-2  Hahnemann Laboratories, INC.    HUMAN OTC DRUG  unapproved homeopathic 
CHLOROQUINE PHOSPHATE 37662-0271-4  Hahnemann Laboratories, INC.    HUMAN OTC DRUG  unapproved homeopathic 
HYDROXYCHLOROQUINE SULFATE 60219-1544-1  Amneal Pharmaceuticals NY LLC  ANDA210577  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 68084-269-11  American Health Packaging  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 0904-7046-06  Major Pharmaceuticals  ANDA210441  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 16571-112-10  Rising Pharma Holdings, Inc.  ANDA210959  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 71335-1771-5  Bryant Ranch Prepack  ANDA040081  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 16729-563-01  Accord Healthcare, Inc.,  ANDA213342  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 68071-2912-2  NuCare Pharmaceuticals,Inc.  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 68788-7747-3  Preferred Pharmaceuticals, Inc.  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 42385-971-01  Laurus Labs Limited  ANDA210959  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 50268-412-11  AvPAK  ANDA210441  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 50090-3432-1  A-S Medication Solutions  NDA009768  HUMAN PRESCRIPTION DRUG  NDA AUTHORIZED GENERIC 
HYDROXYCHLOROQUINE SULFATE 65841-633-05  Zydus Lifesciences Limited  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 50090-5573-2  A-S Medication Solutions  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 71205-448-12  Proficient Rx LP  NDA009768  HUMAN PRESCRIPTION DRUG  NDA 
HYDROXYCHLOROQUINE SULFATE 55154-3567-0  Cardinal Health 107, LLC  ANDA210441  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 68382-096-01  Zydus Pharmaceuticals USA Inc.  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 16714-110-02  Northstar Rx LLC.  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
CHLOROQUINE PHOSPHATE 0115-7010-09  Amneal Pharmaceuticals of New York LLC  ANDA040516  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 16729-485-01  Accord Healthcare, Inc.,  ANDA213342  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 71610-473-53  Aphena Pharma Solutions - Tennessee, LLC  NDA009768  HUMAN PRESCRIPTION DRUG  NDA 
HYDROXYCHLOROQUINE SULFATE 71610-701-53  Aphena Pharma Solutions - Tennessee, LLC  ANDA210441  HUMAN PRESCRIPTION DRUG  ANDA 
CHLOROQUINE PHOSPHATE 64980-178-10  Rising Pharmaceuticals, Inc.  ANDA090612  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 50090-2508-2  A-S Medication Solutions  ANDA040133  HUMAN PRESCRIPTION DRUG  ANDA 
CHLOROQUINE PHOSPHATE 64980-177-01  Rising Pharmaceuticals, Inc.  ANDA091621  HUMAN PRESCRIPTION DRUG  ANDA 
HYDROXYCHLOROQUINE SULFATE 71335-0897-9  Bryant Ranch Prepack  ANDA040657  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-193

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