Package 0338-0719-06

Brand: dextrose

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 0338-0719-06
Digits Only 0338071906
Product NDC 0338-0719
Product ID 0338-0719_aa64f648-e931-4a99-9b81-791a3827272c
Description

2000 mL in 1 BAG (0338-0719-06)

Marketing

Marketing Status
Marketed Since 1991-07-02
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": "aa64f648-e931-4a99-9b81-791a3827272c", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["237656"], "spl_set_id": ["0332f34a-7038-47cc-ba59-d55cad6b73ca"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2000 mL in 1 BAG (0338-0719-06)", "package_ndc": "0338-0719-06", "marketing_start_date": "19910702"}], "brand_name": "DEXTROSE", "product_id": "0338-0719_aa64f648-e931-4a99-9b81-791a3827272c", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0338-0719", "generic_name": "Dextrose monohydrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "70 g/100mL"}], "application_number": "NDA020047", "marketing_category": "NDA", "marketing_start_date": "19910702", "listing_expiration_date": "20261231"}