Divalproex Sodium 125 mg / 1 Tablet 100 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1100832-7122-11
Product NDC00832-7122
Generic Drug NameDivalproex Sodium
Brand NameDivalproex Sodium
ManufacturerUpsher-Smith Laboratories, LLC
Strength125 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Tablet, Delayed Release
Package Description100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-11)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

Divalproex Sodium 125 mg / 1 Tablet is tracked under NDC 00832-7122-11 and rolls up into product family 00832-7122. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 100 Tablet, Delayed Release.
  • Manufacturer: Upsher-Smith Laboratories, LLC.
  • Dosage form: Tablet.
  • Family size: 2 indexed presentations.

Official references

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Alternate presentations in this family

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Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 9 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Hubdivalproex sodium 125 mg / 1 Tablet delayed release 100 Tablet, Delayed Release Bottle10 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex Sodium 125 mg / 1 Tablet 100 Tablet, Delayed Release, NDC 00832-7122-11, is a Upsher-Smith Laboratories, LLC 125 mg / 1 tablet presentation packaged as 100 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 00832-7122-11
  • Digits-only NDC 11: 00832712211
  • Possible 10-digit display format: 0832-7122-11 (0832712211)

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