dobutamine

Generic: dobutamine

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dobutamine
Generic Name dobutamine
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

dobutamine hydrochloride 12.5 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-2344
Product ID 0409-2344_e71e9520-871b-479d-9652-1857fceca863
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074086
Listing Expiration 2026-12-31
Marketing Start 2005-06-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04092344
Hyphenated Format 0409-2344

Supplemental Identifiers

RxCUI
1812168
UNII
0WR771DJXV

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name dobutamine (source: ndc)
Application Number ANDA074086 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-2344-01) / 20 mL in 1 VIAL, SINGLE-DOSE
  • 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-02) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-2344-62)
source: ndc

Packages (2)

0409-2344-01 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-2344-01) / 20 mL in 1 VIAL, SINGLE-DOSE 0409-2344-02 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-02) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-2344-62)

Ingredients (1)

dobutamine hydrochloride (12.5 mg/mL)

Linked Drug Pages (2)

DOBUTAMINE ndc-match (0.9) DOBUTAMINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e71e9520-871b-479d-9652-1857fceca863", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["1812168"], "spl_set_id": ["dc537761-d5f4-488d-24ab-b2bcd2b17b7a"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-2344-01)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-2344-01", "marketing_start_date": "20050803"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-02)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-2344-62)", "package_ndc": "0409-2344-02", "marketing_start_date": "20050629"}], "brand_name": "DOBUTAMINE", "product_id": "0409-2344_e71e9520-871b-479d-9652-1857fceca863", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0409-2344", "generic_name": "DOBUTAMINE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "12.5 mg/mL"}], "application_number": "ANDA074086", "marketing_category": "ANDA", "marketing_start_date": "20050629", "listing_expiration_date": "20261231"}