dobutamine hydrochloride

Generic: dobutamine hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dobutamine hydrochloride
Generic Name dobutamine hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

dobutamine hydrochloride 100 mg/100mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

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
adrenergic beta-agonists [moa] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621566
Hyphenated Format 51662-1566

Supplemental Identifiers

RxCUI
309985
UNII
0WR771DJXV

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/100mL
source: ndc
Packaging
  • 250 mL in 1 BAG (51662-1566-1)
source: ndc

Packages (1)

Ingredients (1)

dobutamine hydrochloride (100 mg/100mL)

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"}