Package 29300-381-05

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 29300-381-05
Digits Only 2930038105
Product NDC 29300-381
Product ID 29300-381_3dc4aa08-e179-49a4-a926-c717cfb5135e
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05)

Marketing

Marketing Status
Marketed Since 2022-07-15
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": "3dc4aa08-e179-49a4-a926-c717cfb5135e", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["1d4129ae-0ce8-4a04-9f9d-c770508de8ed"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-01)", "package_ndc": "29300-381-01", "marketing_start_date": "20220715"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05)", "package_ndc": "29300-381-05", "marketing_start_date": "20220715"}], "brand_name": "divalproex sodium", "product_id": "29300-381_3dc4aa08-e179-49a4-a926-c717cfb5135e", "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": "29300-381", "generic_name": "divalproex sodium", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "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": "20261231"}