Package 71335-0008-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71335-0008-1
Digits Only 7133500081
Product NDC 71335-0008
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)

Marketing

Marketing Status
Marketed Since 2018-12-21
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3cc98db5-a0e2-48ee-bd51-86dddc1c8c5b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["d67af03a-5261-4358-8787-2e729267ff7e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)", "package_ndc": "71335-0008-1", "marketing_start_date": "20181221"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2)", "package_ndc": "71335-0008-2", "marketing_start_date": "20180306"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3)", "package_ndc": "71335-0008-3", "marketing_start_date": "20180301"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4)", "package_ndc": "71335-0008-4", "marketing_start_date": "20211227"}], "brand_name": "Divalproex Sodium", "product_id": "71335-0008_3cc98db5-a0e2-48ee-bd51-86dddc1c8c5b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-0008", "generic_name": "Divalproex Sodium", "labeler_name": "Bryant Ranch Prepack", "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": "20111001", "listing_expiration_date": "20261231"}