FDA Drug Approval, A064053, NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
FDA Drug Approval, A064053, NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
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Contents: Summary Basis of Approval
ANDA: 064053
Company: BAUSCH AND LOMB
Drug Name: NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
Active Ingredients: HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength: 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
Dosage Form/Route: SOLUTION/DROPS;OTIC
Action Date: 12/29/1995
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AT
- 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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