divalproex sodium

Generic: divalproex sodium

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-032
Product ID 71610-032_a117c85f-4dfb-46da-99aa-4c4146e78865
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078182
Listing Expiration 2026-12-31
Marketing Start 2014-03-21

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 71610032
Hyphenated Format 71610-032

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 ANDA078182 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)
source: ndc

Packages (2)

71610-032-53 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53) 71610-032-60 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)

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": "a117c85f-4dfb-46da-99aa-4c4146e78865", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["9cfdcb58-d6d7-43bb-b6e1-17172b143296"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53)", "package_ndc": "71610-032-53", "marketing_start_date": "20180119"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)", "package_ndc": "71610-032-60", "marketing_start_date": "20180119"}], "brand_name": "Divalproex Sodium", "product_id": "71610-032_a117c85f-4dfb-46da-99aa-4c4146e78865", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71610-032", "generic_name": "Divalproex Sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, 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_start_date": "20140321", "listing_expiration_date": "20261231"}