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
- 62756-299_c89dfc75-606c-4a4e-9d2b-d907b492a837
- Product NDC
- 62756-299
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- phenytoin sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080630
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYTOIN SODIUM — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08) · 62756-299-08
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13) · 62756-299-13
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83) · 62756-299-83
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88) · 62756-299-88
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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