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FDA Drug Approval, A085635, DEPO-TESTOSTERONE
FDA Drug Approval, A085635, DEPO-TESTOSTERONE
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ANDA: 085635
Company: PFIZER
Drug Name: DEPO-TESTOSTERONE
Active Ingredients: TESTOSTERONE CYPIONATE
Strength: 200MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 07/25/1979
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AO
Company: PFIZER
Drug Name: DEPO-TESTOSTERONE
Active Ingredients: TESTOSTERONE CYPIONATE
Strength: 200MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 07/25/1979
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AO
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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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