| NDC Code | 57664-170-08 |
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| Package Description | 100 TABLET in 1 BOTTLE (57664-170-08) |
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| Product NDC | 57664-170 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20090330 |
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| End Marketing Date | 20210831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090118 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
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| Strength | 7.5; 325 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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