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