# Simvastatin

NDC: 68084-512
Generic name: Simvastatin
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110908

FDA application: ANDA078103

## 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:"68084-512"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-512
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4bec3923-6221-4b8b-9a72-872a63680de1