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U.S. Department of Health and Human Services

FDA Application

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NDC Search Results on Active Ingredient: Chlorpromazine

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
CHLORPROMAZINE HYDROCHLORIDE 16714-048-01  Northstar Rx LLC  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 0904-7131-61  Major Pharmaceuticals  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1509-1  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1509-4  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 0904-7132-61  Major Pharmaceuticals  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1510-1  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1510-4  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1510-2  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1509-2  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1506-2  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1132-2  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1129-1  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 0904-7129-61  Major Pharmaceuticals  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1131-1  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1129-2  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1131-2  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1132-1  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70710-1133-1  Zydus Pharmaceuticals (USA) Inc.  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 16714-050-01  Northstar Rx LLC  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 70771-1508-2  Zydus Lifesciences Limited  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 16714-049-01  Northstar Rx LLC  ANDA213368  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 23155-805-01  Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.  ANDA213590  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 23155-804-01  Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.  ANDA213590  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 23155-806-01  Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.  ANDA213590  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 23155-807-01  Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.  ANDA213590  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 23155-803-01  Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.  ANDA213590  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 63304-185-10  Sun Pharmaceutical Industries Inc  ANDA214256  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 63304-185-01  Sun Pharmaceutical Industries Inc  ANDA214256  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 63304-114-10  Sun Pharmaceutical Industries Inc  ANDA214256  HUMAN PRESCRIPTION DRUG  ANDA 
CHLORPROMAZINE HYDROCHLORIDE 63304-114-01  Sun Pharmaceutical Industries Inc  ANDA214256  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-239

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