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FDA Drug Approval, N011757, DEPO-MEDROL
FDA Drug Approval, N011757, DEPO-MEDROL
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NDA: 011757
Company: PFIZER
Drug Name: DEPO-MEDROL
Active Ingredients: METHYLPREDNISOLONE ACETATE
Strength: 80MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 05/27/1959
Marketing Status: Prescription
Submission Classification: Type 2 - New Active Ingredient
Company: PFIZER
Drug Name: DEPO-MEDROL
Active Ingredients: METHYLPREDNISOLONE ACETATE
Strength: 80MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 05/27/1959
Marketing Status: Prescription
Submission Classification: Type 2 - New Active Ingredient
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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