# LOSARTAN POTASSIUM

NDC: 42571-112
Generic name: losartan potassium
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20121206

FDA application: ANDA091541

## Active ingredients

- LOSARTAN POTASSIUM: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2f2b6c6-0ab1-483f-b4a2-78dfe3200153