Package 70518-3459-0
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
70518-3459-0
Digits Only
7051834590
Product NDC
70518-3459
Description
100 POUCH in 1 BOX (70518-3459-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3459-1)
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": "3c2e3726-c1f1-b29d-e063-6294a90a161b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["fb8b7710-6827-4fa2-a0a1-d290f533b16b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3459-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3459-1)", "package_ndc": "70518-3459-0", "marketing_end_date": "20270623", "marketing_start_date": "20220725"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3459-2)", "package_ndc": "70518-3459-2", "marketing_end_date": "20270623", "marketing_start_date": "20230709"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3459-3)", "package_ndc": "70518-3459-3", "marketing_end_date": "20270623", "marketing_start_date": "20240926"}], "brand_name": "Divalproex Sodium", "product_id": "70518-3459_3c2e3726-c1f1-b29d-e063-6294a90a161b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3459", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078182", "marketing_category": "ANDA", "marketing_end_date": "20270623", "marketing_start_date": "20220725"}