| NDC Code | 68084-846-25 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-846-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-846-95) |
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| Product NDC | 68084-846 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fluphenazine Hydrochloride |
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| Non-Proprietary Name | Fluphenazine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20141003 |
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| End Marketing Date | 20190531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089742 |
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| Manufacturer | American Health Packaging |
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| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazines [CS],Phenothiazine [EPC] |
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