# Lovastatin

NDC: 50090-0762
Generic name: lovastatin
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071101

FDA application: ANDA078296

## Active ingredients

- LOVASTATIN: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-0762"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-0762
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02aae38d-ee9d-4c09-a155-b69f221ed3e9