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FDA Drug Approval, A211941, CARBOPROST TROMETHAMINE
FDA Drug Approval, A211941, CARBOPROST TROMETHAMINE
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ANDA: 211941
Company: DR REDDYS
Drug Name: CARBOPROST TROMETHAMINE
Active Ingredients: CARBOPROST TROMETHAMINE
Strength: EQ 0.25MG BASE/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 07/02/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AP
Company: DR REDDYS
Drug Name: CARBOPROST TROMETHAMINE
Active Ingredients: CARBOPROST TROMETHAMINE
Strength: EQ 0.25MG BASE/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 07/02/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AP
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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