Divalproex Sodium 250 mg / 1 Tablet 1000 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1162756-0797-18
Product NDC62756-0797
Generic Drug NameDivalproex Sodium
Brand NameDivalproex Sodium
ManufacturerSun Pharmaceutical Industries, Inc.
Strength250 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1000 Tablet, Delayed Release
Package Description1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

Divalproex Sodium 250 mg / 1 Tablet is tracked under NDC 62756-0797-18 and rolls up into product family 62756-0797. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1000 Tablet, Delayed Release.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Tablet.
  • Family size: 5 indexed presentations.

Official references

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Alternate presentations in this family

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Potential alternatives with matching presentation

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View Potential Alternative HubDivalproex Sodium 250 mg / 1 Tablet delayed release 1000 Tablet, Delayed Release Bottle3 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex Sodium 250 mg / 1 Tablet 1000 Tablet, Delayed Release, NDC 62756-0797-18, is a Sun Pharmaceutical Industries, Inc. 250 mg / 1 tablet presentation packaged as 1000 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 62756-0797-18
  • Digits-only NDC 11: 62756079718
  • Possible 10-digit display format: 62756-797-18 (6275679718)

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