Package 50090-7841-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7841-0
Digits Only 5009078410
Product NDC 50090-7841
Product ID 50090-7841_21277d3e-ee56-48ad-a2b2-015dae50b6e9
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0)

Marketing

Marketing Status
Marketed Since 2025-12-29
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": "21277d3e-ee56-48ad-a2b2-015dae50b6e9", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["e5fcf5b1-263e-43e0-9424-e613d5cca3fa"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0)", "package_ndc": "50090-7841-0", "marketing_start_date": "20251229"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-1)", "package_ndc": "50090-7841-1", "marketing_start_date": "20251229"}], "brand_name": "divalproex sodium", "product_id": "50090-7841_21277d3e-ee56-48ad-a2b2-015dae50b6e9", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-7841", "generic_name": "divalproex sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA214643", "marketing_category": "ANDA", "marketing_start_date": "20220225", "listing_expiration_date": "20271231"}