# Simvastatin

NDC: 82009-014
Generic name: Simvastatin
Labeler / Manufacturer: Quallent Pharmaceuticals Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220526

FDA application: ANDA200895

## Active ingredients

- SIMVASTATIN: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82009-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b4255a7-f9f5-4235-8dbb-b0f03acbd624