FDA Drug Approval, A216605, ROPIVACAINE HYDROCHLORIDE

FDA Drug Approval, A216605, ROPIVACAINE HYDROCHLORIDE

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ANDA: 216605
Company: AMNEAL
Drug Name: ROPIVACAINE HYDROCHLORIDE
Active Ingredients: ROPIVACAINE HYDROCHLORIDE
Strength: 1GM/200ML (5MG/ML)
Dosage Form/Route: SOLUTION;INJECTION
Action Date: 03/08/2023
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AP
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