| NDC Code | 54868-5900-0 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-5900-0) |
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| Product NDC | 54868-5900 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dihydrocodeine Bitartrate, Acetaminophen And Caffeine |
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| Non-Proprietary Name | Dihydrocodeine Bitartrate, Acetaminophen And Caffeine |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20080520 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040701 |
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| Manufacturer | Physicians Total Care, Inc. |
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| Substance Name | DIHYDROCODEINE BITARTRATE; ACETAMINOPHEN; CAFFEINE |
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| Strength | 32; 712.8; 60 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
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| DEA Schedule | CIII |
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