| NDC Code | 70710-1129-4 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (70710-1129-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1129-2) |
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| Product NDC | 70710-1129 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Chlorpromazine Hydrochloride |
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| Non-Proprietary Name | Chlorpromazine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20200127 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213368 |
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| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
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| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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