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Dobutamine HclDrug - Dobutamine Hcl The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Dobutamine Hydrochloride
Strength -
EQ 12.5MG BASE/ML
Applicant -
BEDFORD
New Drug Application (NDA) Number -
074277
Product Number -
001
Therapeutic Equivalence (TE) Code -
AP
Approval Date -
Oct 31, 1994
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Bedford Laboratories Div Ben Venue Laboratories Inc
Dobutamine Hcl
Depakote Cp Eq 250mg Base Tablet, Delayed Release; Oral
Depakote Cp Eq 500mg Base Tablet, Delayed Release; Oral Depakote Er Eq 250mg Valproic Acid Tablet, Extended Release; Oral Depakote Er Eq 500mg Valproic Acid Tablet, Extended Release; Oral Dobutamine Hcl Eq 12.5mg Base/ml Injectable; Injection Dobutamine Hcl Eq 12.5mg Base/ml Injectable; Injection Dobutamine Hcl Eq 12.5mg Base/ml Injectable; Injection Depakote Eq 125mg Valproic Acid Tablet, Delayed Release; Oral Depakote Eq 250mg Valproic Acid Tablet, Delayed Release; Oral Depakote Eq 500mg Valproic Acid Tablet, Delayed Release; Oral NewDrugInformation |