| NDC Code | 70069-752-01 |
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| Package Description | 1 VIAL in 1 CARTON (70069-752-01) / 50 mL in 1 VIAL |
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| Product NDC | 70069-752 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bupivacaine Hydrochloride |
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| Non-Proprietary Name | Bupivacaine Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INFILTRATION; PERINEURAL |
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| Start Marketing Date | 20231127 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217792 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | BUPIVACAINE HYDROCHLORIDE |
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| Strength | 2.5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE] |
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