Package 55154-2336-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55154-2336-0
Digits Only 5515423360
Product NDC 55154-2336
Description

10 BLISTER PACK in 1 BAG (55154-2336-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2008-07-29
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01bb5a7a-b488-4676-a3e0-7487a98f4989", "openfda": {"upc": ["0055154415408", "0055154233606"], "unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["5e59609f-d79d-414b-a6fc-7efb1ba5b200"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2336-0)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-2336-0", "marketing_start_date": "20080729"}], "brand_name": "Divalproex Sodium", "product_id": "55154-2336_01bb5a7a-b488-4676-a3e0-7487a98f4989", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-2336", "generic_name": "Divalproex Sodium", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}