Human Drugs View

Product Information DRP-10895_PI_01.pdf
Registration Number DRP-10895
Generic Name Ondansetron (as hydrochloride)
Brand Name Ondi
Dosage Strength 2 mg/mL (4 mg/2 mL)
Dosage Form Solution for Injection (IM/IV)
Classification Prescription Drug (RX)
Pharmacologic Category Antiemetic (5-HT-3-Receptor Antagonist)
Packaging Clear Glass Ampoule x 2 mL and 4 mL (Box of 10's)
Manufacturer Sakar Healthcare Pvt. Ltd.
Country of Origin India
Trader
Importer Macropharma Corporation
Distributor Macropharma Corporation
Application Type Initial
Issuance Date 14 December 2021
Expiry Date 14 December 2026