# ATORVASTATIN CALCIUM

NDC: 82009-004
Generic name: ATORVASTATIN CALCIUM
Labeler / Manufacturer: Quallent
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211123

FDA application: ANDA090548

## Active ingredients

- ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82009-004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f00a83aa-3f1d-566d-b9bb-f396f22a27cb