# Extended Phenytoin Sodium

NDC: 60687-841
Generic name: Phenytoin Sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250206

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:"60687-841"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-841
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5b64cb11-673a-41ec-9b2a-1e194ae5eb0c