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
- 51672-4146_4e03fb7d-d33a-2472-e063-6394a90a9b81
- Product NDC
- 51672-4146
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Phenytoin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140417
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENYTOIN — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-1) · 51672-4146-1
- 1000 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-3) · 51672-4146-3
- 30 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-6) · 51672-4146-6
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 →