Package 0409-6648-02

Brand: dextrose

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 0409-6648-02
Digits Only 0409664802
Product NDC 0409-6648
Product ID 0409-6648_2f05a8f1-4651-405c-a66b-8e96a46c1db8
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6648-16)

Marketing

Marketing Status
Marketed Since 2005-03-31
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": "2f05a8f1-4651-405c-a66b-8e96a46c1db8", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517", "1795514"], "spl_set_id": ["4ed365da-4e62-4329-c1b9-c197ab4fb6e1"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02)  / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6648-16)", "package_ndc": "0409-6648-02", "marketing_start_date": "20050331"}], "brand_name": "Dextrose", "product_id": "0409-6648_2f05a8f1-4651-405c-a66b-8e96a46c1db8", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-6648", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20050331", "listing_expiration_date": "20271231"}