Package 50090-7121-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7121-0
Digits Only 5009071210
Product NDC 50090-7121
Product ID 50090-7121_08b17543-143a-4a15-a132-f9fd48cfa204
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0)

Marketing

Marketing Status
Marketed Since 2024-03-27
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Divalproex Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08b17543-143a-4a15-a132-f9fd48cfa204", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625"], "spl_set_id": ["63d61062-2700-47f4-8ab4-3bd641b81fe1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0)", "package_ndc": "50090-7121-0", "marketing_start_date": "20240327"}], "brand_name": "Divalproex Sodium", "product_id": "50090-7121_08b17543-143a-4a15-a132-f9fd48cfa204", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-7121", "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": "125 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20141024", "listing_expiration_date": "20261231"}