# Griseofulvin

NDC: 0781-5515
Generic name: Griseofulvin
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130807

FDA application: ANDA091592

## Active ingredients

- GRISEOFULVIN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-5515"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-5515
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98829d90-b289-4bec-a625-7af412a5cb2d