Package 50090-4737-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 50090-4737-0
Digits Only 5009047370
Product NDC 50090-4737
Product ID 50090-4737_2edc27fc-04ad-46ad-b2ca-179ca4e62209
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-0)

Marketing

Marketing Status
Marketed Since 2019-11-20
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": "2edc27fc-04ad-46ad-b2ca-179ca4e62209", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["94eac383-a89f-4128-b81c-076640b8edcf"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-0)", "package_ndc": "50090-4737-0", "marketing_start_date": "20191120"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-1)", "package_ndc": "50090-4737-1", "marketing_start_date": "20191120"}], "brand_name": "Divalproex sodium", "product_id": "50090-4737_2edc27fc-04ad-46ad-b2ca-179ca4e62209", "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": "50090-4737", "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": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}