Package 70518-2036-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2036-0
Digits Only 7051820360
Product NDC 70518-2036
Product ID 70518-2036_499b72b7-b905-4be2-e063-6394a90ae98d
Description

100 POUCH in 1 BOX (70518-2036-0) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2036-1)

Marketing

Marketing Status
Marketed Since 2019-04-24
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499b72b7-b905-4be2-e063-6394a90ae98d", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["33f07aac-4dc5-4f97-976a-a84f93497bc6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2036-0)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2036-1)", "package_ndc": "70518-2036-0", "marketing_start_date": "20190424"}], "brand_name": "Divalproex Sodium", "product_id": "70518-2036_499b72b7-b905-4be2-e063-6394a90ae98d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-2036", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "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": "20190424", "listing_expiration_date": "20271231"}