epinephrine

Generic: epinephrine

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name epinephrine
Generic Name epinephrine
Labeler glenmark pharmaceuticals inc., usa
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAMUSCULAR INTRAOCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

epinephrine 1 mg/mL

Manufacturer
GLENMARK PHARMACEUTICALS INC., USA

Identifiers & Regulatory

Product NDC 68462-933
Product ID 68462-933_e77f1aa3-df4b-4129-b72f-e9a4122a8f55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218144
Listing Expiration 2026-12-31
Marketing Start 2025-06-03

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 68462933
Hyphenated Format 68462-933

Supplemental Identifiers

RxCUI
1660014
UPC
0368462933107
UNII
YKH834O4BH
NUI
N0000000209 N0000000245 N0000175552 N0000175555 N0000175570 M0003647

Packaging Origin

Original Packager
true

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 ANDA218144 (source: ndc)
Routes
INTRAMUSCULAR INTRAOCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (68462-933-10) / 1 mL in 1 AMPULE (68462-933-01)
source: ndc

Packages (1)

68462-933-10 10 AMPULE in 1 BOX (68462-933-10) / 1 mL in 1 AMPULE (68462-933-01)

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": "e77f1aa3-df4b-4129-b72f-e9a4122a8f55", "openfda": {"nui": ["N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647"], "upc": ["0368462933107"], "unii": ["YKH834O4BH"], "rxcui": ["1660014"], "spl_set_id": ["01fd19cd-190c-4989-b733-60ba95941297"], "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": ["GLENMARK PHARMACEUTICALS INC., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (68462-933-10)  / 1 mL in 1 AMPULE (68462-933-01)", "package_ndc": "68462-933-10", "marketing_start_date": "20250603"}], "brand_name": "epinephrine", "product_id": "68462-933_e77f1aa3-df4b-4129-b72f-e9a4122a8f55", "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": "68462-933", "generic_name": "epinephrine", "labeler_name": "GLENMARK PHARMACEUTICALS INC., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "epinephrine", "active_ingredients": [{"name": "EPINEPHRINE", "strength": "1 mg/mL"}], "application_number": "ANDA218144", "marketing_category": "ANDA", "marketing_start_date": "20250603", "listing_expiration_date": "20261231"}