Divalproex sodium 500 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1170518-4553-00
Product NDC70518-4553
Generic Drug Namedivalproex sodium
Brand Namedivalproex sodium
ManufacturerRemedyrepack Inc.
Strength500 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated, Extended Release
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4553-0)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

divalproex sodium 500 mg / 1 Tablet is tracked under NDC 70518-4553-00 and rolls up into product family 70518-4553. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated, Extended Release.
  • Manufacturer: Remedyrepack 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 3 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 500 mg / 1 Tablet extended release 30 Tablet, Film Coated, Extended Release Blister3 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex sodium 500 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 70518-4553-00, is a Remedyrepack Inc. 500 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 70518-4553-00
  • Digits-only NDC 11: 70518455300
  • Possible 10-digit display format: 70518-4553-0 (7051845530)

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