# ATORVASTATIN CALCIUM

NDC: 77771-451
Generic name: ATORVASTATIN CALCIUM
Labeler / Manufacturer: Radha Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230810

FDA application: ANDA205519

## Active ingredients

- 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:"77771-451"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-451
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10e766cc-c3fd-4584-a0d7-652c516e828c