# Pravastatin Sodium

NDC: 71205-294
Generic name: Pravastatin Sodium
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060425

FDA application: ANDA076056

## Active ingredients

- PRAVASTATIN SODIUM: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-294"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-294
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=466e2d1a-a6d6-40f8-a9f6-3e7494a34ca6