divalproex sodium

Generic: divalproex sodium

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler lifestar pharma llc
Dosage Form CAPSULE, COATED PELLETS
Routes
ORAL
Active Ingredients

divalproex sodium 125 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-447
Product ID 70756-447_55cf638a-82a6-4df7-a37a-e179f71630dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217358
Listing Expiration 2026-12-31
Marketing Start 2025-08-12

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 70756447
Hyphenated Format 70756-447

Supplemental Identifiers

RxCUI
1099596
UPC
0370756447115 0370756447306 0370756447122 0370756447511
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 ANDA217358 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 100 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-11)
  • 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-12)
  • 30 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-30)
  • 500 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-51)
source: ndc

Packages (4)

70756-447-11 100 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-11) 70756-447-12 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-12) 70756-447-30 30 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-30) 70756-447-51 500 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-51)

Ingredients (1)

divalproex sodium (125 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": "55cf638a-82a6-4df7-a37a-e179f71630dc", "openfda": {"upc": ["0370756447115", "0370756447306", "0370756447122", "0370756447511"], "unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["b2388bfd-7455-48ae-b396-463df0c278f0"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-11)", "package_ndc": "70756-447-11", "marketing_start_date": "20250812"}, {"sample": false, "description": "1000 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-12)", "package_ndc": "70756-447-12", "marketing_start_date": "20250812"}, {"sample": false, "description": "30 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-30)", "package_ndc": "70756-447-30", "marketing_start_date": "20250812"}, {"sample": false, "description": "500 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-51)", "package_ndc": "70756-447-51", "marketing_start_date": "20250812"}], "brand_name": "divalproex sodium", "product_id": "70756-447_55cf638a-82a6-4df7-a37a-e179f71630dc", "dosage_form": "CAPSULE, COATED PELLETS", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70756-447", "generic_name": "divalproex sodium", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA217358", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}