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
- 29300-379_a6527387-ec89-41a1-b85a-c0fb7b4a7db7
- Product NDC
- 29300-379
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Phenytoin Sodium
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221112
- Source listing expiry
- 20261231
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 (29300-379-01) · 29300-379-01
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (29300-379-05) · 29300-379-05
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (29300-379-10) · 29300-379-10
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 →