# Phenytoin Sodium

NDC: 57664-808
Generic name: Phenytoin Sodium
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170724

FDA application: ANDA040684

## 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:"57664-808"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-808
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92e98c47-abba-4018-99b6-a1fffed6db8b