divalproex sodium

Generic: divalproex sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 250 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-797
Product ID 62756-797_044ee7fd-d980-4b48-b2b7-aa1717e44638
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078597
Listing Expiration 2026-12-31
Marketing Start 2008-07-29

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 62756797
Hyphenated Format 62756-797

Supplemental Identifiers

RxCUI
1099625 1099678 1099870
UPC
0362756796836 0362756798830
UNII
644VL95AO6

Packaging Origin

Original Packager
true

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 ANDA078597 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08)
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83)
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88)
source: ndc

Packages (5)

62756-797-08 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08) 62756-797-13 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13) 62756-797-18 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18) 62756-797-83 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83) 62756-797-88 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88)

Ingredients (1)

divalproex sodium (250 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": "044ee7fd-d980-4b48-b2b7-aa1717e44638", "openfda": {"upc": ["0362756796836", "0362756798830"], "unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["64797788-fdcb-4d12-a1a4-743ad71bd17b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08)", "package_ndc": "62756-797-08", "marketing_start_date": "20080729"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13)", "package_ndc": "62756-797-13", "marketing_start_date": "20080729"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)", "package_ndc": "62756-797-18", "marketing_start_date": "20080729"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83)", "package_ndc": "62756-797-83", "marketing_start_date": "20080729"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88)", "package_ndc": "62756-797-88", "marketing_start_date": "20080729"}], "brand_name": "Divalproex Sodium", "product_id": "62756-797_044ee7fd-d980-4b48-b2b7-aa1717e44638", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "62756-797", "generic_name": "Divalproex Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}