| NDC Code | 70069-062-10 |
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| Package Description | 10 VIAL in 1 CARTON (70069-062-10) > 20 mL in 1 VIAL (70069-062-01) |
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| Product NDC | 70069-062 |
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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 |
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| Usage | EPIDURAL; INFILTRATION; PERINEURAL |
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| Start Marketing Date | 20180615 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207636 |
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| Manufacturer | Somerset Therapeutics, 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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