# Phenytoin

NDC: 0904-7199
Generic name: Phenytoin
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20140417

FDA application: ANDA200565

## Active ingredients

- PHENYTOIN: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7199"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7199
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=08a9d26b-4419-43ec-98f3-43d4534c2e76