# PRAVASTATIN SODIUM

NDC: 72162-1951
Generic name: PRAVASTATIN SODIUM
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210201

FDA application: ANDA209869

## Active ingredients

- PRAVASTATIN SODIUM: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1951"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1951
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7b7f5c28-78fa-4625-ad69-4291500e033d