Package 51079-767-08

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 51079-767-08
Digits Only 5107976708
Product NDC 51079-767
Product ID 51079-767_4358cbe3-b1da-4ab0-e063-6394a90afa64
Description

80 BLISTER PACK in 1 CARTON (51079-767-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-767-01)

Marketing

Marketing Status
Marketed Since 2009-02-03
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": "4358cbe3-b1da-4ab0-e063-6394a90afa64", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["b367d81d-4eca-4e28-b490-34be4c003561"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 CARTON (51079-767-08)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-767-01)", "package_ndc": "51079-767-08", "marketing_start_date": "20090203"}], "brand_name": "Divalproex Sodium", "product_id": "51079-767_4358cbe3-b1da-4ab0-e063-6394a90afa64", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "51079-767", "generic_name": "divalproex sodium", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA077567", "marketing_category": "ANDA", "marketing_start_date": "20090203", "listing_expiration_date": "20261231"}