divalproex sodium

Generic: divalproex sodium

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler american health packaging
Dosage Form CAPSULE, COATED PELLETS
Routes
ORAL
Active Ingredients

divalproex sodium 125 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-313
Product ID 68084-313_337704d6-7d3c-1fee-e063-6394a90a664b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078919
Listing Expiration 2026-12-31
Marketing Start 2009-03-18

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 68084313
Hyphenated Format 68084-313

Supplemental Identifiers

RxCUI
1099596
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 ANDA078919 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-313-01) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)
  • 50 BLISTER PACK in 1 CARTON (68084-313-65) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)
source: ndc

Packages (2)

68084-313-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-313-01) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11) 68084-313-65 50 BLISTER PACK in 1 CARTON (68084-313-65) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)

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": "337704d6-7d3c-1fee-e063-6394a90a664b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["2e4778d8-8798-4da1-bb33-1aa1414b5809"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-313-01)  / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)", "package_ndc": "68084-313-01", "marketing_start_date": "20090318"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (68084-313-65)  / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)", "package_ndc": "68084-313-65", "marketing_start_date": "20240626"}], "brand_name": "Divalproex Sodium", "product_id": "68084-313_337704d6-7d3c-1fee-e063-6394a90a664b", "dosage_form": "CAPSULE, COATED PELLETS", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "68084-313", "generic_name": "Divalproex Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA078919", "marketing_category": "ANDA", "marketing_start_date": "20090318", "listing_expiration_date": "20261231"}