# Fluvastatin Sodium

NDC: 0378-8020
Generic name: fluvastatin
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20120411

FDA application: ANDA090595

## Active ingredients

- FLUVASTATIN SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-8020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-8020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0a7247c-5d83-4bc1-840f-c58314d14195