| NDC Code | 0121-0504-04 |
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| Package Description | 118 mL in 1 BOTTLE (0121-0504-04) |
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| Product NDC | 0121-0504 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Acetaminophen And Codeine Phosphate |
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| Non-Proprietary Name | Acetaminophen And Codeine Phosphate |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 19810821 |
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| End Marketing Date | 20250430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA087508 |
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| Manufacturer | PAI Holdings, LLC dba PAI Pharma |
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| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
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| Strength | 120; 12 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CV |
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