# Simvastatin

NDC: 16714-682
Generic name: Simvastatin
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20061220

FDA application: ANDA077691

## Active ingredients

- SIMVASTATIN: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-682"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-682
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0376351b-f1a0-43e5-a0b4-533072c49f39