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 | 0527-2963-37 | Lannett Company, Inc. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7131-61 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7132-61 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7129-61 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7130-61 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7133-61 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0904-7130-06 | Major Pharmaceuticals | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 16714-051-01 | Northstar Rx LLC | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 16714-047-01 | Northstar Rx LLC | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 16714-049-01 | Northstar Rx LLC | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 16714-050-01 | Northstar Rx LLC | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 16714-048-01 | Northstar Rx LLC | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 72205-104-91 | Novadoz Pharmaceuticals LLC | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 72205-107-91 | Novadoz Pharmaceuticals LLC | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 72205-106-91 | Novadoz Pharmaceuticals LLC | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 72205-105-91 | Novadoz Pharmaceuticals LLC | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3510-1 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3086-1 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3549-2 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3086-0 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3280-0 | REMEDYREPACK INC. | ANDA212144 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3673-1 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3952-0 | REMEDYREPACK INC. | ANDA084112 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3510-0 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3086-2 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3590-2 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3348-0 | REMEDYREPACK INC. | ANDA213368 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-0016-2 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3549-1 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3584-0 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
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