# Extended Phenytoin Sodium

NDC: 65862-692
Generic name: Phenytoin Sodium
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20150610

FDA application: ANDA204309

## Active ingredients

- PHENYTOIN SODIUM: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-692"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-692
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5362ea50-38a4-48b4-a85b-d634c3d8b91a