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Timolol Hemihydrate

NDC 70069-697 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216654
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsTIMOLOL ANHYDROUS (5 mg/mL)
Marketing started20241031
Package count1

External sources

Source: openFDA. Public-domain (CC0).