Package 68001-106-00

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 68001-106-00
Digits Only 6800110600
Product NDC 68001-106
Product ID 68001-106_304dd980-5e9b-d776-e063-6394a90aa9cf
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00)

Marketing

Marketing Status
Marketed Since 2013-10-08
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": "304dd980-5e9b-d776-e063-6394a90aa9cf", "openfda": {"upc": ["0368001105002", "0368001106009"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["1b12c694-e120-45f6-ad28-36373e2c5378"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00)", "package_ndc": "68001-106-00", "marketing_start_date": "20131008"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-03)", "package_ndc": "68001-106-03", "marketing_start_date": "20131008"}], "brand_name": "Divalproex Sodium", "product_id": "68001-106_304dd980-5e9b-d776-e063-6394a90aa9cf", "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": "68001-106", "generic_name": "Divalproex Sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078239", "marketing_category": "ANDA", "marketing_start_date": "20131008", "listing_expiration_date": "20261231"}