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Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

Divalproex sodiumNDC Family 65862-0595Divalproex sodium 500 mg / 1
Brand Name: Divalproex sodiumDosage: TabletPackage: 100 Tablet, Film Coated, Extended ReleaseType: Oral
NDC 1165862-0595-01
Product NDC65862-0595
Generic Drug NameDivalproex sodium
Brand NameDivalproex sodium
ManufacturerAurobindo Pharma Limited
Strength500 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Tablet, Film Coated, Extended Release
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-01)
Active IngredientsDivalproex Sodium
Marketing CategoryANDA

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NDC snapshot

Divalproex sodium 500 mg / 1 Tablet is tracked under NDC 65862-0595-01 and rolls up into product family 65862-0595. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 100 Tablet, Film Coated, Extended Release.
  • Manufacturer: Aurobindo Pharma Limited.
  • Dosage form: Tablet.
  • Family size: 3 indexed presentations.

Click a tag to refine the catalog view around this product reference.

NDC Family 65862-0595Presentation: Divalproex sodium 500 mg / 1Dosage: TabletPackage: 100 Tablet, Film Coated, Extended Release
Review the generic familyDivalproex sodium

Official references

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

Search DailyMed labelingOpens DailyMed search results.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Divalproex sodium 500 mg / 1 Tablet 10 Blister PackNDC 65862-0595-10 | 10 Blister Pack | Aurobindo Pharma LimitedDivalproex sodium 500 mg / 1 Tablet 500 Tablet, Film Coated, Extended ReleaseNDC 65862-0595-05 | 500 Tablet, Film Coated, Extended Release | Aurobindo Pharma Limited

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 10 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 100 Tablet, Film Coated, Extended Release Bottle10 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended ReleaseNDC 00378-0473-01 | 100 Tablet, Film Coated, Extended Release | Mylan Pharmaceuticals Inc.Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended ReleaseNDC 16714-0485-01 | 100 Tablet, Film Coated, Extended Release | NorthStar Rx LLCDivalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended ReleaseNDC 29300-0381-01 | 100 Tablet, Film Coated, Extended Release | Unichem Pharmaceuticals (USA), Inc.Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended ReleaseNDC 31722-0022-01 | 100 Tablet, Film Coated, Extended Release | Camber Pharmaceuticals, Inc.Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended ReleaseNDC 63629-4698-04 | 100 Tablet, Film Coated, Extended Release | Bryant Ranch Prepack

Divalproex sodium 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended Release, NDC 65862-0595-01, is a Aurobindo Pharma Limited 500 mg / 1 tablet presentation packaged as 100 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 65862-0595-01
  • Digits-only NDC 11: 65862059501
  • Possible 10-digit display formats: 65862-595-01 (6586259501), 65862-0595-1 (6586205951)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

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