| NDC Code | 16571-889-50 |
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| Package Description | 500 TABLET, FILM COATED in 1 CONTAINER (16571-889-50) |
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| Product NDC | 16571-889 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fluphenazine Hydrochoride |
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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 | 20240607 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA218283 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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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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