dobutamine in dextrose
Generic: dobutamine in dextrose
Labeler: hf acquisition co. llc, dba healthfirstDrug Facts
Product Profile
Brand Name
dobutamine in dextrose
Generic Name
dobutamine in dextrose
Labeler
hf acquisition co. llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dobutamine hydrochloride 100 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1664
Product ID
51662-1664_47bf8f3f-ee08-c235-e063-6394a90a96fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020201
Listing Expiration
2027-12-31
Marketing Start
2005-08-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621664
Hyphenated Format
51662-1664
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 in dextrose (source: ndc)
Generic Name
dobutamine in dextrose (source: ndc)
Application Number
NDA020201 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/100mL
Packaging
- 250 mL in 1 BAG (51662-1664-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "47bf8f3f-ee08-c235-e063-6394a90a96fb", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985"], "spl_set_id": ["3418aa46-2d9a-39f3-e063-6294a90a2961"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1664-1)", "package_ndc": "51662-1664-1", "marketing_start_date": "20050812"}], "brand_name": "DOBUTAMINE IN DEXTROSE", "product_id": "51662-1664_47bf8f3f-ee08-c235-e063-6394a90a96fb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1664", "generic_name": "DOBUTAMINE IN DEXTROSE", "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOBUTAMINE IN DEXTROSE", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "100 mg/100mL"}], "application_number": "NDA020201", "marketing_category": "NDA", "marketing_start_date": "20050812", "listing_expiration_date": "20271231"}