| NDC Code | 71351-022-50 |
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| Package Description | 50 AMPULE in 1 PACKAGE (71351-022-50) / 2 mL in 1 AMPULE (71351-022-02) |
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| Product NDC | 71351-022 |
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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 |
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| Usage | SUBARACHNOID |
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| Start Marketing Date | 20221031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212822 |
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| Manufacturer | Brookfield Pharmaceuticals, LLC. |
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| Substance Name | BUPIVACAINE HYDROCHLORIDE |
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| Strength | 7.5 |
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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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