Ondenget
Brand Name: Ondenget
Generic Name: Ondansetron (as Hydrochloride)
Active
Registration Number
DRP-5894-03
Dosage Form
Solution for Injection (I.M/I.V.)
Issuance Date
April 7, 2024
Expiry Date
December 11, 2029
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength2 mg/mL
PackagingFlint USP Type I Glass Ampoule with Blue Colour Band x 5 mL (4 mL net volume) (Box of 5’s)
Classification
C
Classification
Prescription Drug (Rx)
P
Pharmacologic
Antiemetic
A
Application
Renewal
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Ondansetron (as Hydrochloride)Active
Monograph: Ondansetron