| NDC Code | 68462-865-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68462-865-01) |
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| Product NDC | 68462-865 |
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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 | 20210323 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212144 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
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| Strength | 200 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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