Active Ingredient: GRANISETRON HYDROCHLORIDE
Proprietary Name: GRANISETRON HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202648
Product Number: 001
Approval Date: Jun 29, 2020
Applicant Holder Full Name: YUNG SHIN PHARMACEUTICAL INDUSTRIAL CO LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: GRANISETRON HYDROCHLORIDE
Proprietary Name: GRANISETRON HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202648
Product Number: 002
Approval Date: Jun 29, 2020
Applicant Holder Full Name: YUNG SHIN PHARMACEUTICAL INDUSTRIAL CO LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information