# SIMVASTATIN

NDC: 68180-482
Generic name: SIMVASTATIN
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20090714

FDA application: ANDA078103

## Active ingredients

- SIMVASTATIN: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-482"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-482
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e48217f-8175-4e9b-9fd0-909be4bbba95