# AMLODIPINE AND OLMESARTAN MEDOXOMIL

NDC: 42571-237
Generic name: Amlodipine and Olmesartan Medoxomil
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180101

FDA application: ANDA207435

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- OLMESARTAN MEDOXOMIL: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-237"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-237
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7fcf6a87-7b3e-4cef-8c47-c8a008cfea82