Package 51662-1330-1

Brand: dobutamine

Generic: dobutamine
NDC Package

Package Facts

Identity

Package NDC 51662-1330-1
Digits Only 5166213301
Product NDC 51662-1330
Product ID 51662-1330_100c9203-3714-02bc-e063-6294a90afb2f
Description

250 mL in 1 BAG (51662-1330-1)

Marketing

Marketing Status
Marketed Since 2019-04-07
Brand dobutamine
Generic dobutamine
Sample Package No

Linked Drug Pages (1)

DOBUTAMINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "100c9203-3714-02bc-e063-6294a90afb2f", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309986"], "spl_set_id": ["85fb5ba6-3597-e09f-e053-2a91aa0aded5"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1330-1)", "package_ndc": "51662-1330-1", "marketing_start_date": "20190407"}], "brand_name": "DOBUTAMINE", "product_id": "51662-1330_100c9203-3714-02bc-e063-6294a90afb2f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1330", "generic_name": "DOBUTAMINE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "200 mg/100mL"}], "application_number": "NDA020201", "marketing_category": "NDA", "marketing_start_date": "20190407", "listing_expiration_date": "20261231"}