Active Ingredient: HYDROCORTAMATE HYDROCHLORIDE
Proprietary Name: MAGNACORT
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N010554
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:
Discontinued
Patent and Exclusivity Information