Package 0409-2344-88

Brand: dobutamine

Generic: dobutamine
NDC Package

Package Facts

Identity

Package NDC 0409-2344-88
Digits Only 0409234488
Product NDC 0409-2344
Description

10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-88) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-2344-68)

Marketing

Marketing Status
Marketed Since 2005-04-30
Brand dobutamine
Generic dobutamine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5d6b1dfe-d679-4aea-97a6-3d074a202afe", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["1812168"], "spl_set_id": ["89becb0c-da60-4f43-0a98-29ff7a9eca58"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-88)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-2344-68)", "package_ndc": "0409-2344-88", "marketing_start_date": "20050430"}], "brand_name": "DOBUTAMINE", "product_id": "0409-2344_5d6b1dfe-d679-4aea-97a6-3d074a202afe", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0409-2344", "generic_name": "DOBUTAMINE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "12.5 mg/mL"}], "application_number": "ANDA074086", "marketing_category": "ANDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}