# DILANTIN

NDC: 70518-4325
Generic name: Extended Phenytoin Sodium
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250402

FDA application: ANDA084349

## Active ingredients

- PHENYTOIN SODIUM: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4325"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4325
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db8c69b0-4697-433e-98c7-b0b2d2c52a83