| NDC Code | 0603-2337-32 |
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| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-2337-32) |
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| Product NDC | 0603-2337 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Acetaminophen And Codeine |
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| Non-Proprietary Name | Acetaminophen And Codeine Phosphate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19880930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089990 |
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| Manufacturer | Qualitest Pharmaceuticals |
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| Substance Name | CODEINE PHOSPHATE; ACETAMINOPHEN |
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| Strength | 15; 300 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
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| DEA Schedule | CIII |
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