isoproterenol hydrochloride
Generic: isoproterenol hydrochloride
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
isoproterenol hydrochloride
Generic Name
isoproterenol hydrochloride
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
isoproterenol hydrochloride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-316
Product ID
55150-316_a2c8dee4-69b8-479b-a203-25fdd0c234f1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211864
Listing Expiration
2026-12-31
Marketing Start
2021-02-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150316
Hyphenated Format
55150-316
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA211864 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 25 AMPULE in 1 CARTON (55150-316-25) / 1 mL in 1 AMPULE (55150-316-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRACARDIAC", "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "a2c8dee4-69b8-479b-a203-25fdd0c234f1", "openfda": {"upc": ["0355150317011", "0355150317103"], "unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["3e4050e8-7d94-4ed7-951d-1ff818ddadf1"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (55150-316-25) / 1 mL in 1 AMPULE (55150-316-01)", "package_ndc": "55150-316-25", "marketing_start_date": "20210209"}], "brand_name": "Isoproterenol Hydrochloride", "product_id": "55150-316_a2c8dee4-69b8-479b-a203-25fdd0c234f1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "55150-316", "generic_name": "Isoproterenol Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoproterenol Hydrochloride", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA211864", "marketing_category": "ANDA", "marketing_start_date": "20210209", "listing_expiration_date": "20261231"}