| NDC Code | 61919-114-71 |
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| Package Description | 100 BOTTLE in 1 BOTTLE (61919-114-71) > 120 BOTTLE in 1 BOTTLE (61919-114-72) > 90 BOTTLE in 1 BOTTLE (61919-114-90) > 30 BOTTLE in 1 BOTTLE (61919-114-30) > 15 BOTTLE in 1 BOTTLE (61919-114-15) > 60 TABLET in 1 BOTTLE (61919-114-60) |
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| Product NDC | 61919-114 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20140101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040656 |
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| Manufacturer | Direct Rx |
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| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
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| Strength | 325; 7.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Opioid Agonist [EPC], Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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