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BumetanideDrug - Bumetanide The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Bumetanide
Strength -
0.5MG
Applicant -
SANDOZ
New Drug Application (NDA) Number -
074700
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Nov 21, 1996
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Sandoz Inc
Bumetanide
Bumex 0.25mg/ml Injectable; Injection
Bumetanide 0.5mg Tablet; Oral Bumetanide 1mg Tablet; Oral Bumetanide 2mg Tablet; Oral Bumetanide 0.5mg Tablet; Oral Pulmicort Respules 1mg/2ml Suspension; Inhalation Bumetanide 0.25mg/ml Injectable; Injection Bumetanide 0.25mg/ml Injectable; Injection Bumetanide 0.25mg/ml Injectable; Injection Bumetanide 0.25mg/ml Injectable; Injection NewDrugInformation |