| NDC Code | 60219-1679-1 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-1679-1) |
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| Product NDC | 60219-1679 |
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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 | 20200711 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213647 |
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| Manufacturer | Amneal Pharmaceuticals NY LLC |
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| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
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| Strength | 2.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazines [CS],Phenothiazine [EPC] |
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