Package 31722-021-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 31722-021-01
Digits Only 3172202101
Product NDC 31722-021
Product ID 31722-021_3ceedd19-b7f3-c44c-e063-6294a90afc44
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)

Marketing

Marketing Status
Marketed Since 2023-09-26
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": "3ceedd19-b7f3-c44c-e063-6294a90afc44", "openfda": {"upc": ["0331722022057", "0331722022019", "0331722021012"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["e8e954d4-54e3-491c-867c-b3b656b70f23"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)", "package_ndc": "31722-021-01", "marketing_start_date": "20230926"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-05)", "package_ndc": "31722-021-05", "marketing_start_date": "20230926"}], "brand_name": "Divalproex sodium", "product_id": "31722-021_3ceedd19-b7f3-c44c-e063-6294a90afc44", "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": "31722-021", "generic_name": "Divalproex sodium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA215527", "marketing_category": "ANDA", "marketing_start_date": "20230923", "listing_expiration_date": "20261231"}