Isuprel - 0409-1410-01 - (ISOPROTERENOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of Isuprel

Product NDC: 0409-1410
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: 0409-1410
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010515
Marketing Category: NDA
Start Marketing Date: 20120618

Package Information of Isuprel

Package NDC: 0409-1410-01
Package Description: 25 AMPULE in 1 PACKAGE (0409-1410-01) > 1 mL in 1 AMPULE

NDC Information of Isuprel

NDC Code 0409-1410-01
Proprietary Name Isuprel
Package Description 25 AMPULE in 1 PACKAGE (0409-1410-01) > 1 mL in 1 AMPULE
Product NDC 0409-1410
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 Hospira, Inc.
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


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