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FDA Drug Approval, N207926, PHENYLEPHRINE HYDROCHLORIDE
FDA Drug Approval, N207926, PHENYLEPHRINE HYDROCHLORIDE
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NDA: 207926
Company: ALCON
Drug Name: PHENYLEPHRINE HYDROCHLORIDE
Active Ingredients: PHENYLEPHRINE HYDROCHLORIDE
Strength: SOLUTION/DROPS;OPHTHALMIC
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: AT
Submission Classification: STANDARD
Company: ALCON
Drug Name: PHENYLEPHRINE HYDROCHLORIDE
Active Ingredients: PHENYLEPHRINE HYDROCHLORIDE
Strength: SOLUTION/DROPS;OPHTHALMIC
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: AT
Submission Classification: STANDARD
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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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