# Telmisartan and Amlodipine

NDC: 0378-1075
Generic name: telmisartan and amlodipine
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140919

FDA application: ANDA202516

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- TELMISARTAN: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-1075"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-1075
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca60a4d5-ace7-4889-94ee-e2265fd63811