Package 0409-2347-32

Brand: dobutamine in dextrose

Generic: dobutamine in dextrose
NDC Package

Package Facts

Identity

Package NDC 0409-2347-32
Digits Only 0409234732
Product NDC 0409-2347
Product ID 0409-2347_2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5
Description

12 POUCH in 1 CASE (0409-2347-32) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-2347-31)

Marketing

Marketing Status
Marketed Since 2006-01-20
Brand dobutamine in dextrose
Generic dobutamine in dextrose
Sample Package No

Linked Drug Pages (1)

Dobutamine in Dextrose ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985", "309986", "309987"], "spl_set_id": ["9943a961-3b50-4847-8a84-d8414ce38daa"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0409-2347-32)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-2347-31)", "package_ndc": "0409-2347-32", "marketing_start_date": "20060120"}], "brand_name": "Dobutamine in Dextrose", "product_id": "0409-2347_2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0409-2347", "generic_name": "Dobutamine in Dextrose", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dobutamine in Dextrose", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "200 mg/100mL"}], "application_number": "NDA020201", "marketing_category": "NDA", "marketing_start_date": "20060120", "listing_expiration_date": "20261231"}