dobutamine hydrochloride in dextrose
Generic: dobutamine hydrochloride
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
dobutamine hydrochloride in dextrose
Generic Name
dobutamine hydrochloride
Labeler
baxter healthcare corporation
Dosage Form
INJECTION
Routes
Active Ingredients
dobutamine hydrochloride 100 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-1073
Product ID
0338-1073_34c787c1-46f7-4264-951d-c88a34dca533
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020255
Listing Expiration
2027-12-31
Marketing Start
1993-09-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03381073
Hyphenated Format
0338-1073
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 hydrochloride in dextrose (source: ndc)
Generic Name
dobutamine hydrochloride (source: ndc)
Application Number
NDA020255 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/100mL
Packaging
- 18 BAG in 1 CARTON (0338-1073-02) / 250 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "34c787c1-46f7-4264-951d-c88a34dca533", "openfda": {"unii": ["0WR771DJXV"], "rxcui": ["309985", "309986", "309987"], "spl_set_id": ["6b17b98b-e06d-42ed-925f-69aa2699dead"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 BAG in 1 CARTON (0338-1073-02) / 250 mL in 1 BAG", "package_ndc": "0338-1073-02", "marketing_start_date": "19930927"}], "brand_name": "Dobutamine Hydrochloride in Dextrose", "product_id": "0338-1073_34c787c1-46f7-4264-951d-c88a34dca533", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0338-1073", "generic_name": "Dobutamine Hydrochloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dobutamine Hydrochloride in Dextrose", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "100 mg/100mL"}], "application_number": "NDA020255", "marketing_category": "NDA", "marketing_start_date": "19930927", "listing_expiration_date": "20271231"}