Package 55154-3552-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55154-3552-0
Digits Only 5515435520
Product NDC 55154-3552
Product ID 55154-3552_2a151ab7-6048-4e15-af62-56b0d7406e1c
Description

10 BLISTER PACK in 1 BAG (55154-3552-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-01-23
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Divalproex sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a151ab7-6048-4e15-af62-56b0d7406e1c", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["0816a066-9ee3-4c23-944d-3539fc2c12bf"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3552-0)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-3552-0", "marketing_start_date": "20090123"}], "brand_name": "Divalproex sodium", "product_id": "55154-3552_2a151ab7-6048-4e15-af62-56b0d7406e1c", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-3552", "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": "125 mg/1"}], "application_number": "ANDA078979", "marketing_category": "ANDA", "marketing_start_date": "20090123", "listing_expiration_date": "20261231"}