# Amlodipine and Atorvastatin

NDC: 62332-755
Generic name: Amlodipine and Atorvastatin
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250523

FDA application: ANDA217279

## Active ingredients

- AMLODIPINE BESYLATE: 2.5 mg/1
- ATORVASTATIN CALCIUM TRIHYDRATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-755"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-755
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1346631f-e6db-4c5c-a6af-5aa7b80a011d