Package 55154-2345-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55154-2345-0
Digits Only 5515423450
Product NDC 55154-2345
Product ID 55154-2345_cd7f9ac8-08fa-4278-ae17-254fccf31c2c
Description

10 BLISTER PACK in 1 BAG (55154-2345-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-06-01
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cd7f9ac8-08fa-4278-ae17-254fccf31c2c", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["283af6d2-8ea2-4225-b2e7-a2057dbdb793"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2345-0)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-2345-0", "marketing_start_date": "20150601"}], "brand_name": "Divalproex Sodium", "product_id": "55154-2345_cd7f9ac8-08fa-4278-ae17-254fccf31c2c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-2345", "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": "ANDA203730", "marketing_category": "ANDA", "marketing_start_date": "20150601", "listing_expiration_date": "20261231"}