| NDC Code | 70518-0499-1 |
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| Package Description | 30 mL in 1 VIAL, SINGLE-DOSE (70518-0499-1) |
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| Product NDC | 70518-0499 |
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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 | EPIDURAL; INTRACAUDAL |
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| Start Marketing Date | 20170509 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203895 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | BUPIVACAINE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
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