Divalproex Sodium 125 mg / 1 Tablet 30 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

Divalproex Sodium NDC Family 50090-7635 Divalproex Sodium 125 mg / 1

NDC 11	50090-7635-00
Product NDC	50090-7635
Generic Drug Name	Divalproex Sodium
Brand Name	Divalproex Sodium
Manufacturer	A-S Medication Solutions
Strength	125 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet, Delayed Release
Package Description	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7635-0)
Active Ingredients	Divalproex Sodium
Marketing Category	ANDA

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NDC snapshot

Divalproex Sodium 125 mg / 1 Tablet is tracked under NDC 50090-7635-00 and rolls up into product family 50090-7635. 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: A-S Medication Solutions.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyDivalproex Sodium

Official references

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Potential alternatives with matching presentation

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View Potential Alternative Hubdivalproex sodium 125 mg / 1 Tablet delayed release 30 Tablet, Delayed Release Bottle7 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Divalproex Sodium 125 mg / 1 Tablet 30 Tablet, Delayed Release, NDC 50090-7635-00, is a A-S Medication Solutions 125 mg / 1 tablet presentation packaged as 30 Tablet, Delayed Release.

NDC search formats

Canonical NDC 11: 50090-7635-00
Digits-only NDC 11: 50090763500
Possible 10-digit display format: 50090-7635-0 (5009076350)

Helpful product links

Search by brand name: Divalproex Sodium
NDC 11: 50090-7635-00
Product family NDC: 50090-7635
VA classification code: CN400
VA classification code description: ANTICONVULSANTS
CMOP ID: D0562
VUID: 4006249