# PRAVASTATIN SODIUM

NDC: 71205-149
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: 20110718

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:"71205-149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d2b4607-0a46-4b58-9247-dc448ce258ec