# PRAVASTATIN SODIUM

NDC: 63629-9163
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: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-9163"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-9163
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0641def-425e-4357-a6b6-24ce00424549