| NDC Code | 70512-798-01 |
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| Package Description | 200 mL in 1 BAG (70512-798-01) |
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| Product NDC | 70512-798 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ropivacaine Hydrochloride |
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| Non-Proprietary Name | Ropivacaine Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | EPIDURAL; INFILTRATION; PERINEURAL |
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| Start Marketing Date | 20241201 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212808 |
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| Manufacturer | SOLA Pharmaceuticals, LLC |
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| Substance Name | ROPIVACAINE HYDROCHLORIDE |
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| Strength | 2 |
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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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