| NDC Code | 58118-1439-3 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (58118-1439-3) |
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| Product NDC | 58118-1439 |
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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 | 19871016 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089586 |
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| Manufacturer | Clinical Solutions Wholesale |
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| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
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