| NDC Code | 59385-012-30 |
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| Package Description | 30 POUCH in 1 BOX (59385-012-30) > 1 FILM in 1 POUCH (59385-012-01) |
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| Product NDC | 59385-012 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bunavail |
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| Non-Proprietary Name | Buprenorphine And Naloxone |
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| Dosage Form | FILM |
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| Usage | BUCCAL |
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| Start Marketing Date | 20140930 |
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| End Marketing Date | 20210228 |
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| Marketing Category Name | NDA |
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| Application Number | NDA205637 |
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| Manufacturer | BioDelivery Sciences International, Inc. |
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| Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE |
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| Strength | 2.1; .3 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
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| DEA Schedule | CIII |
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