adrenalin (epinephrine)
Generic: adrenalin (epinephrine)
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
adrenalin (epinephrine)
Generic Name
adrenalin (epinephrine)
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
epinephrine 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1290
Product ID
51662-1290_120003b7-8ffd-a631-e063-6394a90a2c0b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA204200
Listing Expiration
2026-12-31
Marketing Start
2018-09-21
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621290
Hyphenated Format
51662-1290
Supplemental Identifiers
RxCUI
UNII
NUI
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
adrenalin (epinephrine) (source: ndc)
Generic Name
adrenalin (epinephrine) (source: ndc)
Application Number
NDA204200 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 mL in 1 VIAL, SINGLE-DOSE (51662-1290-1)
- 25 POUCH in 1 CASE (51662-1290-3) / 1 mL in 1 POUCH (51662-1290-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "SUBCUTANEOUS"], "spl_id": "120003b7-8ffd-a631-e063-6394a90a2c0b", "openfda": {"nui": ["N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647"], "unii": ["YKH834O4BH"], "rxcui": ["1660014"], "spl_set_id": ["7663c49d-1b1d-755d-e053-2991aa0a4ee3"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_epc": ["alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]", "Catecholamine [EPC]"], "pharm_class_moa": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1290-1)", "package_ndc": "51662-1290-1", "marketing_start_date": "20180921"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1290-3) / 1 mL in 1 POUCH (51662-1290-2)", "package_ndc": "51662-1290-3", "marketing_start_date": "20200429"}], "brand_name": "ADRENALIN (EPINEPHRINE)", "product_id": "51662-1290_120003b7-8ffd-a631-e063-6394a90a2c0b", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Catecholamine [EPC]", "Catecholamines [CS]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1290", "generic_name": "ADRENALIN (EPINEPHRINE)", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ADRENALIN (EPINEPHRINE)", "active_ingredients": [{"name": "EPINEPHRINE", "strength": "1 mg/mL"}], "application_number": "NDA204200", "marketing_category": "NDA", "marketing_start_date": "20180921", "listing_expiration_date": "20261231"}