Active Ingredient: HALOPROGIN
Proprietary Name: HALOTEX
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016942
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WESTWOOD SQUIBB PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information