# PRAVASTATIN SODIUM

NDC: 71610-879
Generic name: PRAVASTATIN SODIUM
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110718

FDA application: ANDA076341

## Active ingredients

- PRAVASTATIN SODIUM: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-879"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-879
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e5cfae8-20b8-1fea-e063-6394a90a4e17