| NDC Code | 12496-0757-1 |
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| Package Description | 5 AMPULE in 1 CARTON (12496-0757-1) > 1 mL in 1 AMPULE |
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| Product NDC | 12496-0757 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Buprenex |
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| Non-Proprietary Name | Buprenorphine Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 19850630 |
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| Marketing Category Name | NDA |
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| Application Number | NDA018401 |
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| Manufacturer | Reckitt Benckiser Pharmaceuticals Inc |
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| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
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| Strength | .3 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
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| DEA Schedule | CIII |
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