FDA Drug Approval, A086195, PROCTOFOAM HC
FDA Drug Approval, A086195, PROCTOFOAM HC
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ANDA: 086195
Company: MYLAN SPECIALITY LP
Drug Name: PROCTOFOAM HC
Active Ingredients: HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Strength: 1%;1%
Dosage Form/Route: AEROSOL, METERED;TOPICAL
Action Date: 07/26/1978
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: BX
Company: MYLAN SPECIALITY LP
Drug Name: PROCTOFOAM HC
Active Ingredients: HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Strength: 1%;1%
Dosage Form/Route: AEROSOL, METERED;TOPICAL
Action Date: 07/26/1978
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: BX
- 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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