dopamine hydrochloride
Generic: dopamine hydrochloride
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
dopamine hydrochloride
Generic Name
dopamine hydrochloride
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
dopamine hydrochloride 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-820
Product ID
84549-820_45b0729e-529a-02f6-e063-6294a90a31d3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018132
Listing Expiration
2026-12-31
Marketing Start
2005-08-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549820
Hyphenated Format
84549-820
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
dopamine hydrochloride (source: ndc)
Generic Name
dopamine hydrochloride (source: ndc)
Application Number
NDA018132 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 5 mL in 1 VIAL, SINGLE-DOSE (84549-820-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "45b0729e-529a-02f6-e063-6294a90a31d3", "openfda": {"unii": ["7L3E358N9L"], "rxcui": ["1743941"], "spl_set_id": ["45b0729e-529b-02f6-e063-6294a90a31d3"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (84549-820-01)", "package_ndc": "84549-820-01", "marketing_start_date": "20251211"}], "brand_name": "DOPamine Hydrochloride", "product_id": "84549-820_45b0729e-529a-02f6-e063-6294a90a31d3", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "84549-820", "generic_name": "Dopamine Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOPamine Hydrochloride", "active_ingredients": [{"name": "DOPAMINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "NDA018132", "marketing_category": "NDA", "marketing_start_date": "20050825", "listing_expiration_date": "20261231"}