| NDC Code | 68084-422-01 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (68084-422-01) > 10 TABLET in 1 BLISTER PACK (68084-422-11) |
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| Product NDC | 68084-422 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20100528 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA080439 |
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| Manufacturer | American Health Packaging |
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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 [Chemical/Ingredient] |
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