divalproex sodium

Generic: divalproex sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler proficient rx lp
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-743
Product ID 63187-743_ea6ad932-2a45-4117-9f1d-b21d2b0a1905
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079163
Listing Expiration 2026-12-31
Marketing Start 2011-10-01

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 63187743
Hyphenated Format 63187-743

Supplemental Identifiers

RxCUI
1099678 1099870
UPC
0363187742300 0363187743901
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 ANDA079163 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)
source: ndc

Packages (3)

63187-743-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30) 63187-743-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60) 63187-743-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)

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": "ea6ad932-2a45-4117-9f1d-b21d2b0a1905", "openfda": {"upc": ["0363187742300", "0363187743901"], "unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["abac11e6-7ce1-491c-9ac3-61f3df54c4a4"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30)", "package_ndc": "63187-743-30", "marketing_start_date": "20161003"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60)", "package_ndc": "63187-743-60", "marketing_start_date": "20161003"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)", "package_ndc": "63187-743-90", "marketing_start_date": "20161003"}], "brand_name": "Divalproex Sodium", "product_id": "63187-743_ea6ad932-2a45-4117-9f1d-b21d2b0a1905", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "63187-743", "generic_name": "Divalproex Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}