| NDC Code | 51672-4235-1 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (51672-4235-1) |
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| Product NDC | 51672-4235 |
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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 | 20220414 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215674 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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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 | Phenothiazine [EPC], Phenothiazines [CS] |
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