# Fluvastatin Sodium

NDC: 0093-7446
Generic name: Fluvastatin Sodium
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160602

FDA application: ANDA079011

## Active ingredients

- FLUVASTATIN SODIUM: 80 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-7446"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7446
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc55110f-1ad6-4f97-840d-62b3a5ac415a