Package 65162-757-50

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 65162-757-50
Digits Only 6516275750
Product NDC 65162-757
Product ID 65162-757_4f772f94-d6d3-4b83-9115-b192f4738401
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-50)

Marketing

Marketing Status
Marketed Since 2015-06-01
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": "4f772f94-d6d3-4b83-9115-b192f4738401", "openfda": {"upc": ["0365162755107", "0365162757101"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["7d3352ee-a240-43ff-a243-29ad2bc989c7"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-10)", "package_ndc": "65162-757-10", "marketing_start_date": "20150601"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-50)", "package_ndc": "65162-757-50", "marketing_start_date": "20150601"}], "brand_name": "Divalproex Sodium", "product_id": "65162-757_4f772f94-d6d3-4b83-9115-b192f4738401", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "65162-757", "generic_name": "Divalproex Sodium", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA203730", "marketing_category": "ANDA", "marketing_start_date": "20150601", "listing_expiration_date": "20271231"}