Package 70518-3620-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-3620-0
Digits Only 7051836200
Product NDC 70518-3620
Product ID 70518-3620_4598cf77-7c1d-65d4-e063-6294a90a37d6
Description

100 POUCH in 1 BOX (70518-3620-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)

Marketing

Marketing Status
Marketed Since 2023-01-21
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4598cf77-7c1d-65d4-e063-6294a90a37d6", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["adb813c0-661e-4cf3-abe0-c102dd29cf76"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3620-0)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)", "package_ndc": "70518-3620-0", "marketing_start_date": "20230121"}], "brand_name": "Divalproex Sodium", "product_id": "70518-3620_4598cf77-7c1d-65d4-e063-6294a90a37d6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3620", "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": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20230121", "listing_expiration_date": "20261231"}