| NDC Code | 70934-139-30 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (70934-139-30) |
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| Product NDC | 70934-139 |
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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 | 20181016 |
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| End Marketing Date | 20230430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA083426 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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