Divalproex Sodium 250 mg / 1 Tablet 60 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1168071-3553-06
Product NDC68071-3553
Generic Drug NameDivalproex Sodium
Brand NameDivalproex Sodium
ManufacturerNuCare Pharmaceuticals,Inc.
Strength250 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity60 Tablet, Delayed Release
Package Description60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

Divalproex Sodium 250 mg / 1 Tablet is tracked under NDC 68071-3553-06 and rolls up into product family 68071-3553. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 60 Tablet, Delayed Release.
  • Manufacturer: NuCare Pharmaceuticals,Inc..
  • Dosage form: Tablet.
  • Family size: 1 indexed presentation.

Official references

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

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 7 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 250 mg / 1 Tablet delayed release 60 Tablet, Delayed Release Bottle7 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex Sodium 250 mg / 1 Tablet 60 Tablet, Delayed Release, NDC 68071-3553-06, is a NuCare Pharmaceuticals,Inc. 250 mg / 1 tablet presentation packaged as 60 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 68071-3553-06
  • Digits-only NDC 11: 68071355306
  • Possible 10-digit display format: 68071-3553-6 (6807135536)

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