Package 0904-6861-90

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 0904-6861-90
Digits Only 0904686190
Product NDC 0904-6861
Product ID 0904-6861_946b4453-7cb3-4bb5-b9ca-cdf732af2ca0
Description

90 BLISTER PACK in 1 CARTON (0904-6861-90) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2008-07-29
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": "946b4453-7cb3-4bb5-b9ca-cdf732af2ca0", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["fb39a94e-93e6-4afe-a300-f80e8f1e0fa6"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6861-61)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6861-61", "marketing_start_date": "20080729"}, {"sample": false, "description": "90 BLISTER PACK in 1 CARTON (0904-6861-90)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6861-90", "marketing_start_date": "20080729"}], "brand_name": "Divalproex Sodium", "product_id": "0904-6861_946b4453-7cb3-4bb5-b9ca-cdf732af2ca0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0904-6861", "generic_name": "Divalproex Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}