dopamine hydrochloride
Generic: dopamine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
dopamine hydrochloride
Generic Name
dopamine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
dopamine hydrochloride 40 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621489
Hyphenated Format
51662-1489
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
ANDA207707 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
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
Packages (2)
Ingredients (1)
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"}