Divalproex Sodium 250 mg / 1 Tablet 30 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1167046-1571-03
Product NDC67046-1571
Generic Drug NameDivalproex Sodium
Brand NameDivalproex Sodium
ManufacturerCoupler LLC
Strength250 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Delayed Release
Package Description30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

Divalproex Sodium 250 mg / 1 Tablet is tracked under NDC 67046-1571-03 and rolls up into product family 67046-1571. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Delayed Release.
  • Manufacturer: Coupler LLC.
  • 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 5 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 30 Tablet, Delayed Release Blister6 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex Sodium 250 mg / 1 Tablet 30 Tablet, Delayed Release, NDC 67046-1571-03, is a Coupler LLC 250 mg / 1 tablet presentation packaged as 30 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 67046-1571-03
  • Digits-only NDC 11: 67046157103
  • Possible 10-digit display format: 67046-1571-3 (6704615713)

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