United States · FDA National Drug Code directory
Phenytoin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 59762-0531_212141a3-fffd-49e0-96d5-57cc921a99d1
- Product NDC
- 59762-0531
- Form
- SUSPENSION
- Composition / generic term
- Phenytoin
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20200422
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYTOIN — 125 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (59762-0531-2) / 237 mL in 1 BOTTLE, PLASTIC · 59762-0531-2
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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