| NDC Code | 0472-1630-04 |
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| Package Description | 118 mL in 1 BOTTLE (0472-1630-04) |
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| Product NDC | 0472-1630 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prometh With Dextromethorphan |
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| Non-Proprietary Name | Promethazine Hydrochloride, Dextromethorphan Hydrobromide |
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| Dosage Form | SYRUP |
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| Usage | ORAL |
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| Start Marketing Date | 20070103 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088762 |
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| Manufacturer | Actavis Mid Atlantic LLC |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE |
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| Strength | 6.25; 15 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient],Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA] |
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