# Pravastatin sodium

NDC: 70518-4339
Generic name: Pravastatin sodium
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250513

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:"70518-4339"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4339
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa152ce7-6c07-4aaf-9374-932ce81d0cf9