dopamine hydrochloride

Generic: dopamine hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dopamine hydrochloride
Generic Name dopamine hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

dopamine hydrochloride 40 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1489
Product ID 51662-1489_1203d038-6c4b-4a7c-e063-6294a90a0b73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207707
Listing Expiration 2026-12-31
Marketing Start 2021-08-07

Pharmacologic Class

Classes
catecholamine [epc] catecholamines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621489
Hyphenated Format 51662-1489

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 ANDA207707 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 5 mL in 1 VIAL, SINGLE-DOSE (51662-1489-1)
  • 25 POUCH in 1 CASE (51662-1489-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1489-2) / 5 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

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": "1203d038-6c4b-4a7c-e063-6294a90a0b73", "openfda": {"unii": ["7L3E358N9L"], "rxcui": ["1743941"], "spl_set_id": ["c901b461-4f98-da0a-e053-2a95a90a106e"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (51662-1489-1)", "package_ndc": "51662-1489-1", "marketing_start_date": "20210807"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1489-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1489-2)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1489-3", "marketing_start_date": "20230110"}], "brand_name": "DOPAMINE HYDROCHLORIDE", "product_id": "51662-1489_1203d038-6c4b-4a7c-e063-6294a90a0b73", "dosage_form": "INJECTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "51662-1489", "generic_name": "DOPAMINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOPAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DOPAMINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA207707", "marketing_category": "ANDA", "marketing_start_date": "20210807", "listing_expiration_date": "20261231"}