| NDC Code | 70069-027-05 |
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| Package Description | 5 VIAL in 1 CARTON (70069-027-05) / 1 mL in 1 VIAL |
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| Product NDC | 70069-027 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Buprenorphine Hydrochloride |
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| Non-Proprietary Name | Buprenorphine Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20250211 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA219302 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
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| Strength | .324 |
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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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