# Lovastatin

NDC: 50090-3881
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: 20021125

FDA application: ANDA075991

## Active ingredients

- LOVASTATIN: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-3881"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-3881
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd7a223e-7fc5-4eb0-9bd7-2f9a2d6b4173