Package 51662-1566-1

Brand: dobutamine hydrochloride

Generic: dobutamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1566-1
Digits Only 5166215661
Product NDC 51662-1566
Product ID 51662-1566_1035c14e-d1ea-8603-e063-6394a90a430b
Description

250 mL in 1 BAG (51662-1566-1)

Marketing

Marketing Status
Marketed Since 2021-07-10
Brand dobutamine hydrochloride
Generic dobutamine hydrochloride
Sample Package No

Linked Drug Pages (1)

DOBUTAMINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1035c14e-d1ea-8603-e063-6394a90a430b", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985"], "spl_set_id": ["c6ceb8d3-e46e-f0da-e053-2995a90a8c3c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1566-1)", "package_ndc": "51662-1566-1", "marketing_start_date": "20210710"}], "brand_name": "DOBUTAMINE HYDROCHLORIDE", "product_id": "51662-1566_1035c14e-d1ea-8603-e063-6394a90a430b", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1566", "generic_name": "DOBUTAMINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "100 mg/100mL"}], "application_number": "NDA020255", "marketing_category": "NDA", "marketing_start_date": "20210710", "listing_expiration_date": "20261231"}