| NDC Code | 57664-107-18 |
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| Package Description | 1000 TABLET in 1 BOTTLE (57664-107-18) |
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| Product NDC | 57664-107 |
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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 | 20090127 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040863 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | PROMETHAZINE HYDROCHLORIDE |
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| Strength | 12.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [CS] |
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