# Phenytoin Sodium

NDC: 0641-6139
Generic name: Phenytoin Sodium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 19750716

FDA application: ANDA084307

## Active ingredients

- PHENYTOIN SODIUM: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6139"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6139
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ad1be7b-a1a4-4a2a-bf9b-d22b350aa6e7