Divalproex Sodium 250 mg / 1 Tablet 100 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

Divalproex Sodium NDC Family 72789-0353 Divalproex Sodium 250 mg / 1

NDC 11	72789-0353-01
Product NDC	72789-0353
Generic Drug Name	Divalproex Sodium
Brand Name	Divalproex Sodium
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Strength	250 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	100 Tablet, Delayed Release
Package Description	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01)
Active Ingredients	Divalproex Sodium
Marketing Category	ANDA

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NDC snapshot

Divalproex Sodium 250 mg / 1 Tablet is tracked under NDC 72789-0353-01 and rolls up into product family 72789-0353. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 100 Tablet, Delayed Release.
Manufacturer: PD-Rx Pharmaceuticals, Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyDivalproex Sodium

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Divalproex Sodium 250 mg / 1 Tablet 100 Tablet, Delayed Release, NDC 72789-0353-01, is a PD-Rx Pharmaceuticals, Inc. 250 mg / 1 tablet presentation packaged as 100 Tablet, Delayed Release.

NDC search formats

Canonical NDC 11: 72789-0353-01
Digits-only NDC 11: 72789035301
Possible 10-digit display formats: 72789-353-01 (7278935301), 72789-0353-1 (7278903531)

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.

Helpful product links

Search by brand name: Divalproex Sodium
Exact NDC 11: 72789-0353-01
Product family NDC: 72789-0353
VA classification code: CN400
VA classification code description: ANTICONVULSANTS
CMOP ID: D0564
VUID: 4006250