Package 16714-484-02

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 16714-484-02
Digits Only 1671448402
Product NDC 16714-484
Product ID 16714-484_ef1358b1-4134-47e7-a61a-12fae692225f
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-02)

Marketing

Marketing Status
Marketed Since 2014-06-02
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": "ef1358b1-4134-47e7-a61a-12fae692225f", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["aab6b411-11e9-4a16-afb6-d471ba4756e9"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-01)", "package_ndc": "16714-484-01", "marketing_start_date": "20140602"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-02)", "package_ndc": "16714-484-02", "marketing_start_date": "20140602"}], "brand_name": "Divalproex sodium", "product_id": "16714-484_ef1358b1-4134-47e7-a61a-12fae692225f", "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": "16714-484", "generic_name": "Divalproex sodium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}