# Pravastatin Sodium

NDC: 70518-2505
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: 20191224
Marketing ended: 20260930
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:"70518-2505"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2505
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7e400611-7432-4911-8662-1f0a740f76bb