# PRAVASTATIN SODIUM

NDC: 82009-006
Generic name: PRAVASTATIN SODIUM
Labeler / Manufacturer: Quallent
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211203

FDA application: ANDA076341

## Active ingredients

- PRAVASTATIN SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82009-006"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-006
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9c188f7-cd6f-afac-b493-36552d86589e