DELEXARD
Brand Name: DELEXARD
Generic Name: DOBUTAMINE (as hydrochloride)
Active
Registration Number
DRP-8132-01
Dosage Form
Solution For IV Injection
Issuance Date
May 31, 2024
Expiry Date
April 28, 2029
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength50 mg/mL (250 mg/5 mL)
Packaging5 mL Type I clear and colorless glass ampoule in PVC
tray (Box of 5's)
Classification
C
Classification
Prescription Drug (RX)
P
Pharmacologic
Adrenergic Agent
A
Application
Renewal
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
DOBUTAMINE (as hydrochloride)Active
Monograph: dobutamine (as hydrochloride)