divalproex sodium

Generic: divalproex sodium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler bryant ranch prepack
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2158
Product ID 71335-2158_5079c7a7-f979-4b2e-a516-be3c8a9edc03
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090554
Listing Expiration 2026-12-31
Marketing Start 2014-10-24

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 713352158
Hyphenated Format 71335-2158

Supplemental Identifiers

RxCUI
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 ANDA090554 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)
  • 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)
  • 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)
source: ndc

Packages (5)

71335-2158-1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1) 71335-2158-2 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2) 71335-2158-3 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3) 71335-2158-4 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4) 71335-2158-5 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)

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": "5079c7a7-f979-4b2e-a516-be3c8a9edc03", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["fbaff0ae-431e-4e83-81c2-41eb4b18ee87"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)", "package_ndc": "71335-2158-1", "marketing_start_date": "20220811"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)", "package_ndc": "71335-2158-2", "marketing_start_date": "20230302"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)", "package_ndc": "71335-2158-3", "marketing_start_date": "20220811"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)", "package_ndc": "71335-2158-4", "marketing_start_date": "20240906"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)", "package_ndc": "71335-2158-5", "marketing_start_date": "20220920"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2158_5079c7a7-f979-4b2e-a516-be3c8a9edc03", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2158", "generic_name": "Divalproex Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20141024", "listing_expiration_date": "20261231"}