divalproex sodium

Generic: divalproex sodium

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler cardinal health 107, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-5633
Product ID 55154-5633_3a075f09-76eb-44f9-a892-7d5c302ef0a0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078182
Marketing Start 2014-03-21
Marketing End 2027-08-31

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 551545633
Hyphenated Format 55154-5633

Supplemental Identifiers

RxCUI
1099870
UPC
0055154563307
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 ANDA078182 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-5633-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

55154-5633-0 10 BLISTER PACK in 1 BAG (55154-5633-0) / 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": "3a075f09-76eb-44f9-a892-7d5c302ef0a0", "openfda": {"upc": ["0055154563307"], "unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["4fc50afb-67f3-4bf3-9ec3-cc12734f47fd"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-5633-0)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-5633-0", "marketing_end_date": "20270831", "marketing_start_date": "20160401"}], "brand_name": "Divalproex Sodium", "product_id": "55154-5633_3a075f09-76eb-44f9-a892-7d5c302ef0a0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-5633", "generic_name": "Divalproex Sodium", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078182", "marketing_category": "ANDA", "marketing_end_date": "20270831", "marketing_start_date": "20140321"}