Package 65219-458-30

Brand: dextrose

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 65219-458-30
Digits Only 6521945830
Product NDC 65219-458
Product ID 65219-458_efc3b0c9-518a-47db-bb3e-ebdfd4646e9b
Description

30 BAG in 1 CASE (65219-458-30) / 250 mL in 1 BAG (65219-458-05)

Marketing

Marketing Status
Marketed Since 2024-07-09
Brand dextrose
Generic dextrose monohydrate
Sample Package No

Linked Drug Pages (1)

Dextrose ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "efc3b0c9-518a-47db-bb3e-ebdfd4646e9b", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795607", "1795609", "1795610", "1795612", "1795616"], "spl_set_id": ["576a22d8-5f2f-497e-80ad-1842ca74bb53"], "manufacturer_name": ["FRESENIUS KABI USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CASE (65219-458-30)  / 250 mL in 1 BAG (65219-458-05)", "package_ndc": "65219-458-30", "marketing_start_date": "20240709"}], "brand_name": "Dextrose", "product_id": "65219-458_efc3b0c9-518a-47db-bb3e-ebdfd4646e9b", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "65219-458", "generic_name": "Dextrose Monohydrate", "labeler_name": "FRESENIUS KABI USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "50 mg/mL"}], "application_number": "ANDA207449", "marketing_category": "ANDA", "marketing_start_date": "20240709", "listing_expiration_date": "20261231"}