isoproterenol hydrochloride

Generic: isoproterenol hydrochloride

Labeler: nordic pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name isoproterenol hydrochloride
Generic Name isoproterenol hydrochloride
Labeler nordic pharma, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRACARDIAC INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

isoproterenol hydrochloride .2 mg/mL

Manufacturer
Nordic Pharma, Inc.

Identifiers & Regulatory

Product NDC 69918-731
Product ID 69918-731_1cae2126-a6a9-498c-8fc2-4fb075426f8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211237
Listing Expiration 2026-12-31
Marketing Start 2024-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69918731
Hyphenated Format 69918-731

Supplemental Identifiers

RxCUI
1667909 1667915
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 ANDA211237 (source: ndc)
Routes
INTRACARDIAC INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (69918-731-11) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

69918-731-11 10 VIAL, SINGLE-DOSE in 1 CARTON (69918-731-11) / 1 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

isoproterenol hydrochloride (.2 mg/mL)

Linked Drug Pages (2)

Isoproterenol Hydrochloride ndc-match (0.9) Isoproterenol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRACARDIAC", "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "1cae2126-a6a9-498c-8fc2-4fb075426f8f", "openfda": {"unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["124f44db-b6ba-4886-bfc7-8c71e60ac5b4"], "manufacturer_name": ["Nordic Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (69918-731-11)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "69918-731-11", "marketing_start_date": "20240601"}], "brand_name": "Isoproterenol Hydrochloride", "product_id": "69918-731_1cae2126-a6a9-498c-8fc2-4fb075426f8f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "69918-731", "generic_name": "Isoproterenol Hydrochloride", "labeler_name": "Nordic Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoproterenol Hydrochloride", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA211237", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}