| NDC Code | 0093-5721-56 |
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| Package Description | 30 TABLET in 1 BOTTLE (0093-5721-56) |
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| Product NDC | 0093-5721 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Buprenorphine And Naloxone |
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| Non-Proprietary Name | Buprenorphine And Naloxone |
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| Dosage Form | TABLET |
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| Usage | SUBLINGUAL |
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| Start Marketing Date | 20141210 |
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| End Marketing Date | 20181031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091149 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE |
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| Strength | 8; 2 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
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| DEA Schedule | CIII |
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