dobutamine hydrochloride
Generic: dobutamine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
dobutamine hydrochloride
Generic Name
dobutamine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
dobutamine hydrochloride 100 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1566
Product ID
51662-1566_1035c14e-d1ea-8603-e063-6394a90a430b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020255
Listing Expiration
2026-12-31
Marketing Start
2021-07-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621566
Hyphenated Format
51662-1566
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dobutamine hydrochloride (source: ndc)
Generic Name
dobutamine hydrochloride (source: ndc)
Application Number
NDA020255 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/100mL
Packaging
- 250 mL in 1 BAG (51662-1566-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}