Isuprel - 55154-6988-8 - (ISOPROTERENOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of Isuprel

Product NDC: 55154-6988
Proprietary Name: Isuprel
Non Proprietary Name: ISOPROTERENOL HYDROCHLORIDE
Active Ingredient(s): .2    mg/mL & nbsp;   ISOPROTERENOL HYDROCHLORIDE
Administration Route(s): INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Isuprel

Product NDC: 55154-6988
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010515
Marketing Category: NDA
Start Marketing Date: 20120618

Package Information of Isuprel

Package NDC: 55154-6988-8
Package Description: 1 AMPULE in 1 BAG (55154-6988-8) > 1 mL in 1 AMPULE

NDC Information of Isuprel

NDC Code 55154-6988-8
Proprietary Name Isuprel
Package Description 1 AMPULE in 1 BAG (55154-6988-8) > 1 mL in 1 AMPULE
Product NDC 55154-6988
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ISOPROTERENOL HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20120618
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name ISOPROTERENOL HYDROCHLORIDE
Strength Number .2
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC]

Complete Information of Isuprel


General Information