| NDC Code | 68462-335-14 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (68462-335-14) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 68462-335 |
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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 | 20231106 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216350 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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