# Timolol Hemihydrate

NDC: 70069-697
Generic name: Timolol Hemihydrate
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20241031

FDA application: ANDA216654

## Active ingredients

- TIMOLOL ANHYDROUS: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-697"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-697
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cebc9a5e-0bdb-4f23-9b2c-cde543b62fb6