United States · FDA National Drug Code directory
Phenytoin Sodium
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
- 51672-4111_4d4421be-75f8-2639-e063-6294a90accd5
- Product NDC
- 51672-4111
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Phenytoin Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060905
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENYTOIN SODIUM — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-1) · 51672-4111-1
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-3) · 51672-4111-3
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-6) · 51672-4111-6
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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