Package 51662-1664-1

Brand: dobutamine in dextrose

Generic: dobutamine in dextrose
NDC Package

Package Facts

Identity

Package NDC 51662-1664-1
Digits Only 5166216641
Product NDC 51662-1664
Product ID 51662-1664_47bf8f3f-ee08-c235-e063-6394a90a96fb
Description

250 mL in 1 BAG (51662-1664-1)

Marketing

Marketing Status
Marketed Since 2005-08-12
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": "47bf8f3f-ee08-c235-e063-6394a90a96fb", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985"], "spl_set_id": ["3418aa46-2d9a-39f3-e063-6294a90a2961"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1664-1)", "package_ndc": "51662-1664-1", "marketing_start_date": "20050812"}], "brand_name": "DOBUTAMINE IN DEXTROSE", "product_id": "51662-1664_47bf8f3f-ee08-c235-e063-6394a90a96fb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1664", "generic_name": "DOBUTAMINE IN DEXTROSE", "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE IN DEXTROSE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "100 mg/100mL"}], "application_number": "NDA020201", "marketing_category": "NDA", "marketing_start_date": "20050812", "listing_expiration_date": "20271231"}