| NDC Code | 68047-720-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (68047-720-01) |
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| Product NDC | 68047-720 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Acetaminophen, Caffeine And Dihydrocodeine Bitartrate |
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| Non-Proprietary Name | Acetaminophen, Caffeine And Dihydrocodeine Bitartrate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20161004 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204209 |
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| Manufacturer | Larken Laboratories Inc. |
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| Substance Name | ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE |
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| Strength | 325; 30; 16 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
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| DEA Schedule | CIII |
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