| NDC Code | 57664-146-31 |
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| Package Description | 118 mL in 1 BOTTLE (57664-146-31) |
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| Product NDC | 57664-146 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20090313 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040891 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 6.25 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
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