| NDC Code | 60687-430-65 |
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| Package Description | 50 BLISTER PACK in 1 CARTON (60687-430-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11) |
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| Product NDC | 60687-430 |
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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 | 20190516 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209755 |
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| Manufacturer | American Health Packaging |
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| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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