| NDC Code | 63304-561-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (63304-561-05) |
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| Product NDC | 63304-561 |
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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 | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19800123 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA087083 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
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| Strength | 300; 60 |
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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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