# Lovastatin

NDC: 68001-314
Generic name: lovastatin
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071101

FDA application: ANDA078296

## Active ingredients

- LOVASTATIN: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-314"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-314
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7b86160d-74a9-4774-b5b3-5641e686991f