isoproterenol hydrochloride

Generic: isoproterenol hydrochloride

Labeler: nexus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name isoproterenol hydrochloride
Generic Name isoproterenol hydrochloride
Labeler nexus pharmaceuticals llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

isoproterenol hydrochloride .2 mg/mL

Manufacturer
Nexus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 14789-011
Product ID 14789-011_3ef21b9c-b314-713e-e063-6394a90a9e86
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206961
Listing Expiration 2026-12-31
Marketing Start 2017-08-03

Pharmacologic Class

Classes
adrenergic beta-agonists [moa] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14789011
Hyphenated Format 14789-011

Supplemental Identifiers

RxCUI
1667909 1667915
UPC
0314789011011
UNII
DIA2A74855

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 isoproterenol hydrochloride (source: ndc)
Generic Name isoproterenol hydrochloride (source: ndc)
Application Number ANDA206961 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (14789-011-01) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

14789-011-01 10 VIAL, SINGLE-DOSE in 1 CARTON (14789-011-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

isoproterenol hydrochloride (.2 mg/mL)

Linked Drug Pages (1)

Isoproterenol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3ef21b9c-b314-713e-e063-6394a90a9e86", "openfda": {"upc": ["0314789011011"], "unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["dfb97590-dcbf-47e7-bbfe-f01580eb6ed0"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (14789-011-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "14789-011-01", "marketing_start_date": "20170803"}], "brand_name": "Isoproterenol Hydrochloride", "product_id": "14789-011_3ef21b9c-b314-713e-e063-6394a90a9e86", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "14789-011", "generic_name": "Isoproterenol Hydrochloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoproterenol Hydrochloride", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA206961", "marketing_category": "ANDA", "marketing_start_date": "20170803", "listing_expiration_date": "20261231"}