United States · FDA National Drug Code directory
Dilantin-125
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
- 58151-115_f339f9e4-b289-4efe-82b9-46c57d1dc277
- Product NDC
- 58151-115
- Form
- SUSPENSION
- Composition / generic term
- Phenytoin
- Labeler
- Viatris Specialty LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20240419
- 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 (58151-115-35) / 237 mL in 1 BOTTLE, PLASTIC · 58151-115-35
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →