# AMLODIPINE and OLMESARTAN medoxomil

NDC: 33342-192
Generic name: AMLODIPINE and OLMESARTAN medoxomil
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20161027

FDA application: ANDA206884

## Active ingredients

- AMLODIPINE BESYLATE: 10 mg/1
- OLMESARTAN MEDOXOMIL: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c86a3c45-c906-46c9-9f7b-6c3d89bbe48f