Package 70518-1558-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-1558-0
Digits Only 7051815580
Product NDC 70518-1558
Description

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-1558-0)

Marketing

Marketing Status
Marketed Since 2018-10-19
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494c73bd-6cb6-c2e3-e063-6294a90a86b5", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["cf15569c-5010-4e9b-aef0-7df4de5ed04e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-1558-0)", "package_ndc": "70518-1558-0", "marketing_start_date": "20181019"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-1558-1)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-1558-2)", "package_ndc": "70518-1558-1", "marketing_start_date": "20191016"}], "brand_name": "Divalproex Sodium", "product_id": "70518-1558_494c73bd-6cb6-c2e3-e063-6294a90a86b5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-1558", "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": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20181019", "listing_expiration_date": "20271231"}