Phenytoin sodium 200 mg / 1 Capsule 500 Capsule, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1162756-0299-13
Product NDC62756-0299
Generic Drug Namephenytoin sodium
Brand Namephenytoin sodium
ManufacturerSun Pharmaceutical Industries, Inc.
Strength200 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity500 Capsule, Extended Release
Package Description500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13)
Active IngredientsPhenytoin Sodium
Marketing CategoryANDA

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NDC snapshot

phenytoin sodium 200 mg / 1 Capsule is tracked under NDC 62756-0299-13 and rolls up into product family 62756-0299. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 500 Capsule, Extended Release.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Capsule.
  • Family size: 4 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Phenytoin sodium 200 mg / 1 Capsule 500 Capsule, Extended Release, NDC 62756-0299-13, is a Sun Pharmaceutical Industries, Inc. 200 mg / 1 capsule presentation packaged as 500 Capsule, Extended Release.

NDC search formats

  • Canonical NDC 11: 62756-0299-13
  • Digits-only NDC 11: 62756029913
  • Possible 10-digit display format: 62756-299-13 (6275629913)

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