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 |
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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 |
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