dopamine hydrochloride

Generic: dopamine hydrochloride

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dopamine hydrochloride
Generic Name dopamine hydrochloride
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

dopamine hydrochloride 40 mg/mL

Manufacturer
ProPharma Distribution

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
catecholamine [epc] catecholamines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549820
Hyphenated Format 84549-820

Supplemental Identifiers

RxCUI
1743941
UNII
7L3E358N9L

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 5 mL in 1 VIAL, SINGLE-DOSE (84549-820-01)
source: ndc

Packages (1)

Ingredients (1)

dopamine hydrochloride (40 mg/mL)

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"}