# Amlodipine and atorvastatin

NDC: 0378-4516
Generic name: Amlodipine and atorvastatin
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20141010

FDA application: ANDA200465

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- ATORVASTATIN CALCIUM TRIHYDRATE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-4516"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-4516
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4be76756-4114-4d50-a36c-fd410f6c773d