dobutamine in dextrose
Generic: dobutamine in dextrose
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
dobutamine in dextrose
Generic Name
dobutamine in dextrose
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dobutamine hydrochloride 200 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-2347
Product ID
0409-2347_2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020201
Listing Expiration
2026-12-31
Marketing Start
2006-01-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04092347
Hyphenated Format
0409-2347
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 in dextrose (source: ndc)
Generic Name
dobutamine in dextrose (source: ndc)
Application Number
NDA020201 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/100mL
Packaging
- 12 POUCH in 1 CASE (0409-2347-32) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-2347-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985", "309986", "309987"], "spl_set_id": ["9943a961-3b50-4847-8a84-d8414ce38daa"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0409-2347-32) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-2347-31)", "package_ndc": "0409-2347-32", "marketing_start_date": "20060120"}], "brand_name": "Dobutamine in Dextrose", "product_id": "0409-2347_2cd41f69-c1ea-44a0-9b56-b6f9d963f6a5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0409-2347", "generic_name": "Dobutamine in Dextrose", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dobutamine in Dextrose", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "200 mg/100mL"}], "application_number": "NDA020201", "marketing_category": "NDA", "marketing_start_date": "20060120", "listing_expiration_date": "20261231"}