divalproex sodium

Generic: divalproex sodium

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler major pharmaceuticals
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6861
Product ID 0904-6861_946b4453-7cb3-4bb5-b9ca-cdf732af2ca0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078597
Listing Expiration 2026-12-31
Marketing Start 2008-07-29

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 09046861
Hyphenated Format 0904-6861

Supplemental Identifiers

RxCUI
1099678 1099870
UNII
644VL95AO6

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 divalproex sodium (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number ANDA078597 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6861-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
  • 90 BLISTER PACK in 1 CARTON (0904-6861-90) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

0904-6861-61 100 BLISTER PACK in 1 CARTON (0904-6861-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK 0904-6861-90 90 BLISTER PACK in 1 CARTON (0904-6861-90) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Ingredients (1)

divalproex sodium (500 mg/1)

Linked Drug Pages (1)

Divalproex Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "946b4453-7cb3-4bb5-b9ca-cdf732af2ca0", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["fb39a94e-93e6-4afe-a300-f80e8f1e0fa6"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6861-61)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6861-61", "marketing_start_date": "20080729"}, {"sample": false, "description": "90 BLISTER PACK in 1 CARTON (0904-6861-90)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6861-90", "marketing_start_date": "20080729"}], "brand_name": "Divalproex Sodium", "product_id": "0904-6861_946b4453-7cb3-4bb5-b9ca-cdf732af2ca0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0904-6861", "generic_name": "Divalproex Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}