Zukastop
Brand Name: Zukastop
Generic Name: Ondansetron (as Hydrochloride)
Active
Registration Number
DRP-5894-02
Dosage Form
Solution For Injection (IM/IV)
Issuance Date
April 16, 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 Color
Band x 2 mL (2 mL net volume) (Box of 5's) Flint USP Type I Glass Ampoule with Blue Color 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