divalproex sodium

Generic: divalproex sodium

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler northstar rx llc
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 125 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-260
Product ID 72603-260_7306e665-f551-db56-f79a-624d7cd1225b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078979
Listing Expiration 2026-12-31
Marketing Start 2024-08-01

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 72603260
Hyphenated Format 72603-260

Supplemental Identifiers

RxCUI
1099596
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 divalproex sodium (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number ANDA078979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-01)
  • 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-02)
source: ndc

Packages (2)

72603-260-01 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-01) 72603-260-02 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-02)

Ingredients (1)

divalproex sodium (125 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": "7306e665-f551-db56-f79a-624d7cd1225b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["589ae3a6-8b2e-d931-d36b-1937287ab5c0"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-01)", "package_ndc": "72603-260-01", "marketing_start_date": "20240801"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-02)", "package_ndc": "72603-260-02", "marketing_start_date": "20240801"}], "brand_name": "Divalproex sodium", "product_id": "72603-260_7306e665-f551-db56-f79a-624d7cd1225b", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72603-260", "generic_name": "Divalproex sodium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA078979", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}