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FDA Drug Approval, A040058, PROCHLORPERAZINE
FDA Drug Approval, A040058, PROCHLORPERAZINE
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Contents: Summary Basis of Approval
ANDA: 040058
Company: COSETTE
Drug Name: PROCHLORPERAZINE
Active Ingredients: PROCHLORPERAZINE
Strength: 25MG
Dosage Form/Route: SUPPOSITORY;RECTAL
Action Date: 11/24/1993
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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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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