# Pravastatin Sodium

NDC: 55154-5370
Generic name: Pravastatin Sodium
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120210
Marketing ended: 20260831
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:"55154-5370"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-5370
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca779f66-4b9d-41da-ad0e-e4f58db9fbac