| NDC Code | 0121-1542-40 |
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| Package Description | 4 TRAY in 1 CASE (0121-1542-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 7.5 mL in 1 CUP, UNIT-DOSE (0121-1542-07) |
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| Product NDC | 0121-1542 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zamicet |
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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 | 20080818 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040834 |
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| Manufacturer | Pharmaceutical Associates, Inc. |
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| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
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| Strength | 5; 163 |
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| Strength Unit | mg/7.5mL; mg/7.5mL |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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