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 | 70518-3670-0 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3590-0 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3435-0 | REMEDYREPACK INC. | ANDA212144 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3510-2 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3674-0 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3670-1 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3584-2 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-0016-1 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3584-1 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3674-1 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-0016-0 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3549-0 | REMEDYREPACK INC. | ANDA214827 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3590-1 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3674-2 | REMEDYREPACK INC. | ANDA084113 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 70518-3673-0 | REMEDYREPACK INC. | ANDA212996 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0781-4027-53 | Sandoz, Inc. | ANDA214542 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 0781-4028-22 | Sandoz, Inc. | ANDA214542 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-143-10 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-083-10 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-122-01 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-122-10 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-143-01 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-083-01 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-185-10 | Sun Pharmaceutical Industries Inc | ANDA214256 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 63304-114-01 | 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 | 64725-1397-1 | TYA Pharmaceuticals | ANDA083329 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 64725-5914-1 | TYA Pharmaceuticals | ANDA084112 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPROMAZINE HYDROCHLORIDE | 64725-5916-1 | TYA Pharmaceuticals | ANDA084114 | HUMAN PRESCRIPTION DRUG | ANDA |
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