Package 17856-0109-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 17856-0109-1
Digits Only 1785601091
Product NDC 17856-0109
Product ID 17856-0109_387b221c-08a3-7861-e063-6294a90a1f4e
Description

100 POUCH in 1 BOX (17856-0109-1) / 1 CAPSULE, COATED PELLETS in 1 POUCH

Marketing

Marketing Status
Marketed Since 2021-01-28
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": "387b221c-08a3-7861-e063-6294a90a1f4e", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["699a9722-27bd-4e90-819b-d4ecb99466c8"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (17856-0109-1)  / 1 CAPSULE, COATED PELLETS in 1 POUCH", "package_ndc": "17856-0109-1", "marketing_start_date": "20210128"}], "brand_name": "divalproex sodium", "product_id": "17856-0109_387b221c-08a3-7861-e063-6294a90a1f4e", "dosage_form": "CAPSULE, COATED PELLETS", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "17856-0109", "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": "125 mg/1"}], "application_number": "ANDA078919", "marketing_category": "ANDA", "marketing_start_date": "20190131", "listing_expiration_date": "20261231"}