Package 70518-1138-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-1138-0
Digits Only 7051811380
Product NDC 70518-1138
Product ID 70518-1138_485b18b2-590d-9ff6-e063-6394a90ab1c4
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1138-0)

Marketing

Marketing Status
Marketed Since 2018-04-25
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": "485b18b2-590d-9ff6-e063-6394a90ab1c4", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["74a9f020-f7a1-44e2-a452-f0e37bd3e077"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1138-0)", "package_ndc": "70518-1138-0", "marketing_start_date": "20180425"}], "brand_name": "Divalproex Sodium", "product_id": "70518-1138_485b18b2-590d-9ff6-e063-6394a90ab1c4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-1138", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA090161", "marketing_category": "ANDA", "marketing_start_date": "20180425", "listing_expiration_date": "20271231"}