depakote er

Generic: divalproex sodium

Labeler: abbvie inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name depakote er
Generic Name divalproex sodium
Labeler abbvie inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 250 mg/1

Manufacturer
AbbVie Inc.

Identifiers & Regulatory

Product NDC 0074-7401
Product ID 0074-7401_59a7fe63-4d4b-41da-b586-c51f0bd28509
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021168
Listing Expiration 2027-12-31
Marketing Start 2000-08-04

Pharmacologic Class

Classes
anti-epileptic agent [epc] decreased central nervous system disorganized electrical activity [pe] mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00747401
Hyphenated Format 0074-7401

Supplemental Identifiers

RxCUI
1099563 1099565 1099569 1099571
UPC
0300747402137 0300747401130
UNII
644VL95AO6

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name depakote er (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number NDA021168 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7401-13)
source: ndc

Packages (1)

0074-7401-13 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7401-13)

Ingredients (1)

divalproex sodium (250 mg/1)

Linked Drug Pages (1)

Depakote ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "59a7fe63-4d4b-41da-b586-c51f0bd28509", "openfda": {"upc": ["0300747402137", "0300747401130"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099565", "1099569", "1099571"], "spl_set_id": ["0dc024ce-efc8-4690-7cb5-639c728fccac"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7401-13)", "package_ndc": "0074-7401-13", "marketing_start_date": "20000804"}], "brand_name": "Depakote ER", "product_id": "0074-7401_59a7fe63-4d4b-41da-b586-c51f0bd28509", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0074-7401", "generic_name": "Divalproex Sodium", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Depakote", "brand_name_suffix": "ER", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "NDA021168", "marketing_category": "NDA", "marketing_start_date": "20000804", "listing_expiration_date": "20271231"}