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FDA Drug Approval, N018086, TIMOPTIC
FDA Drug Approval, N018086, TIMOPTIC
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NDA: 018086
Company: BAUSCH AND LOMB INC
Drug Name: TIMOPTIC
Active Ingredients: TIMOLOL MALEATE
Strength: EQ 0.5% BASE
Dosage Form/Route: SOLUTION/DROPS;OPHTHALMIC
Action Date: 08/17/1978
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
Company: BAUSCH AND LOMB INC
Drug Name: TIMOPTIC
Active Ingredients: TIMOLOL MALEATE
Strength: EQ 0.5% BASE
Dosage Form/Route: SOLUTION/DROPS;OPHTHALMIC
Action Date: 08/17/1978
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
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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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