| NDC Code | 0603-5439-21 |
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| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0603-5439-21) |
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| Product NDC | 0603-5439 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Promethazine Hydrochloride |
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| Non-Proprietary Name | Promethazine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20060718 |
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| End Marketing Date | 20180928 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040622 |
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| Manufacturer | Qualitest Pharmaceuticals |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
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