| NDC Code | 25021-652-30 |
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| Package Description | 1 VIAL in 1 CARTON (25021-652-30) > 30 mL in 1 VIAL |
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| Product NDC | 25021-652 |
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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 | 20140923 |
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| End Marketing Date | 20190531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090318 |
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| Manufacturer | Sagent Pharmaceuticals |
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| Substance Name | ROPIVACAINE 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 [CS],Local Anesthesia [PE] |
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