Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOLOL MALEATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.25% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074667
Product Number: 001
Approval Date: Mar 25, 1997
Applicant Holder Full Name: E FOUGERA DIV ALTANA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
