| NDC Code | 0121-0655-04 |
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| Package Description | 118 mL in 1 BOTTLE (0121-0655-04) |
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| Product NDC | 0121-0655 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20110101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040182 |
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| Manufacturer | Pharmaceutical Associates, Inc. |
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| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
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| Strength | 167; 2.5 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CIII |
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