# Pravastatin Sodium

NDC: 50090-0975
Generic name: Pravastatin Sodium
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070511

FDA application: ANDA077987

## 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:"50090-0975"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-0975
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a75de063-c751-4647-bb9e-d4050c1e31fc