Package 81469-492-01
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
81469-492-01
Digits Only
8146949201
Product NDC
81469-492
Description
100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01)
Marketing
Marketing Status
Brand
divalproex sodium
Generic
divalproex sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04436591-edfc-44f9-9813-cf04136c727a", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["a76f9909-28c9-4eb7-8ffd-ff6222fea079"], "manufacturer_name": ["First Nation Group, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01)", "package_ndc": "81469-492-01", "marketing_start_date": "20251110"}, {"sample": false, "description": "1000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10)", "package_ndc": "81469-492-10", "marketing_start_date": "20251110"}], "brand_name": "divalproex sodium", "product_id": "81469-492_04436591-edfc-44f9-9813-cf04136c727a", "dosage_form": "CAPSULE, COATED PELLETS", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "81469-492", "generic_name": "divalproex sodium", "labeler_name": "First Nation Group, 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": "20251110", "listing_expiration_date": "20261231"}