FDA Drug Approval, A208569, TERIPARATIDE

FDA Drug Approval, A208569, TERIPARATIDE

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ANDA: 208569
Company: TEVA PHARMS USA
Drug Name: TERIPARATIDE
Active Ingredients: TERIPARATIDE
Strength: 0.6MG/2.4ML (0.25MG/ML)
Dosage Form/Route: SOLUTION;SUBCUTANEOUS
Action Date: 11/16/2023
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AP
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