epinephrine

Generic: epinephrine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name epinephrine
Generic Name epinephrine
Labeler a-s medication solutions
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAMUSCULAR INTRAOCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

epinephrine 1 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3039
Product ID 50090-3039_f5379d23-2409-4aec-8ccb-0ee72a3f56a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA205029
Listing Expiration 2026-12-31
Marketing Start 2014-08-08

Pharmacologic Class

Established (EPC)
alpha-adrenergic agonist [epc] beta-adrenergic agonist [epc] catecholamine [epc]
Mechanism of Action
adrenergic alpha-agonists [moa] adrenergic beta-agonists [moa]
Chemical Structure
catecholamines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903039
Hyphenated Format 50090-3039

Supplemental Identifiers

RxCUI
1660014
UNII
YKH834O4BH
NUI
N0000000209 N0000000245 N0000175552 N0000175555 N0000175570 M0003647

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 epinephrine (source: ndc)
Generic Name epinephrine (source: ndc)
Application Number NDA205029 (source: ndc)
Routes
INTRAMUSCULAR INTRAOCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 mL in 1 AMPULE (50090-3039-1)
source: ndc

Packages (1)

50090-3039-1 1 mL in 1 AMPULE (50090-3039-1)

Ingredients (1)

epinephrine (1 mg/mL)

Linked Drug Pages (1)

Epinephrine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAOCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "f5379d23-2409-4aec-8ccb-0ee72a3f56a5", "openfda": {"nui": ["N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647"], "unii": ["YKH834O4BH"], "rxcui": ["1660014"], "spl_set_id": ["386519ba-7a44-4edd-9eb1-748419b7a71b"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 AMPULE (50090-3039-1)", "package_ndc": "50090-3039-1", "marketing_start_date": "20170606"}], "brand_name": "Epinephrine", "product_id": "50090-3039_f5379d23-2409-4aec-8ccb-0ee72a3f56a5", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Catecholamine [EPC]", "Catecholamines [CS]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "50090-3039", "generic_name": "Epinephrine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Epinephrine", "active_ingredients": [{"name": "EPINEPHRINE", "strength": "1 mg/mL"}], "application_number": "NDA205029", "marketing_category": "NDA", "marketing_start_date": "20140808", "listing_expiration_date": "20261231"}