# Atorvastatin Calcium

NDC: 42385-941
Generic name: Atorvastatin Calcium
Labeler / Manufacturer: Laurus Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240123

FDA application: ANDA214513

## Active ingredients

- ATORVASTATIN CALCIUM TRIHYDRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42385-941"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42385-941
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f8ca507-b784-4d18-8d3e-d7d68072c416