Active Ingredient: GEMCITABINE HYDROCHLORIDE
Proprietary Name: GEMCITABINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 200MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A204520
Product Number: 001
Approval Date: Jan 5, 2016
Applicant Holder Full Name: GLAND PHARMA LTD
Marketing Status:
Prescription
Patent and Exclusivity Information