Package 55154-5633-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55154-5633-0
Digits Only 5515456330
Product NDC 55154-5633
Product ID 55154-5633_3a075f09-76eb-44f9-a892-7d5c302ef0a0
Description

10 BLISTER PACK in 1 BAG (55154-5633-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-08-31
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": "3a075f09-76eb-44f9-a892-7d5c302ef0a0", "openfda": {"upc": ["0055154563307"], "unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["4fc50afb-67f3-4bf3-9ec3-cc12734f47fd"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-5633-0)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-5633-0", "marketing_end_date": "20270831", "marketing_start_date": "20160401"}], "brand_name": "Divalproex Sodium", "product_id": "55154-5633_3a075f09-76eb-44f9-a892-7d5c302ef0a0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-5633", "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": "ANDA078182", "marketing_category": "ANDA", "marketing_end_date": "20270831", "marketing_start_date": "20140321"}