| NDC Code | 58118-0119-8 |
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| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0119-8) |
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| Product NDC | 58118-0119 |
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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 | 19880812 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089804 |
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| Manufacturer | Clinical Solutions Wholesale, LLC |
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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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