depakote

Generic: divalproex sodium

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

Drug Facts

Product Profile

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

divalproex sodium 500 mg/1

Manufacturer
AbbVie Inc.

Identifiers & Regulatory

Product NDC 0074-7327
Product ID 0074-7327_80bf221b-3559-4141-aa4e-63858690536f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018723
Listing Expiration 2027-12-31
Marketing Start 1983-03-10

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 00747327
Hyphenated Format 0074-7327

Supplemental Identifiers

RxCUI
1099625 1099626 1099678 1099679 1099870 1099871
UPC
0300747326136 0300747327133 0300747325139
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 (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number NDA018723 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7327-13)
source: ndc

Packages (1)

0074-7327-13 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7327-13)

Ingredients (1)

divalproex sodium (500 mg/1)

Linked Drug Pages (1)

Depakote ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "80bf221b-3559-4141-aa4e-63858690536f", "openfda": {"upc": ["0300747326136", "0300747327133", "0300747325139"], "unii": ["644VL95AO6"], "rxcui": ["1099625", "1099626", "1099678", "1099679", "1099870", "1099871"], "spl_set_id": ["08a65cf4-7749-4ceb-6895-8f4805e2b01f"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7327-13)", "package_ndc": "0074-7327-13", "marketing_start_date": "19830310"}], "brand_name": "Depakote", "product_id": "0074-7327_80bf221b-3559-4141-aa4e-63858690536f", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0074-7327", "generic_name": "Divalproex Sodium", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Depakote", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "NDA018723", "marketing_category": "NDA", "marketing_start_date": "19830310", "listing_expiration_date": "20271231"}