Package 17856-0797-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 17856-0797-1
Digits Only 1785607971
Product NDC 17856-0797
Description

100 POUCH in 1 BOX, UNIT-DOSE (17856-0797-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH

Marketing

Marketing Status
Marketed Since 2018-11-02
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": "3852f152-7d42-e53d-e063-6394a90aef95", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["57b71a0b-c2bf-4326-9c26-0f2fe56bf5bc"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (17856-0797-1)  / 1 TABLET, DELAYED RELEASE in 1 POUCH", "package_ndc": "17856-0797-1", "marketing_start_date": "20181102"}], "brand_name": "Divalproex Sodium", "product_id": "17856-0797_3852f152-7d42-e53d-e063-6394a90aef95", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "17856-0797", "generic_name": "Divalproex Sodium", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}