isoproterenol hydrochloride
Generic: isoproterenol hydrochloride
Labeler: amphastar pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
isoproterenol hydrochloride
Generic Name
isoproterenol hydrochloride
Labeler
amphastar pharmaceuticals, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
isoproterenol hydrochloride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0548-9502
Product ID
0548-9502_03384075-bc26-4df6-b1e3-0e20e8808d65
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210106
Listing Expiration
2026-12-31
Marketing Start
2018-07-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05489502
Hyphenated Format
0548-9502
Supplemental Identifiers
RxCUI
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
ANDA210106 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 10 VIAL in 1 CARTON (0548-9502-00) / 5 mL in 1 VIAL
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": "03384075-bc26-4df6-b1e3-0e20e8808d65", "openfda": {"unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["86b2455a-0489-405e-bd0b-9f79d3c5350d"], "manufacturer_name": ["Amphastar Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0548-9502-00) / 5 mL in 1 VIAL", "package_ndc": "0548-9502-00", "marketing_start_date": "20180716"}], "brand_name": "ISOPROTERENOL HYDROCHLORIDE", "product_id": "0548-9502_03384075-bc26-4df6-b1e3-0e20e8808d65", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0548-9502", "generic_name": "Isoproterenol Hydrochloride", "labeler_name": "Amphastar Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ISOPROTERENOL HYDROCHLORIDE", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA210106", "marketing_category": "ANDA", "marketing_start_date": "20180716", "listing_expiration_date": "20261231"}