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: Yes
TE Code: AP
Application Number: A202485
Product Number: 001
Approval Date: May 7, 2013
Applicant Holder Full Name: JIANGSU HANSOH PHARMACEUTICAL GROUP CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: GEMCITABINE HYDROCHLORIDE
Proprietary Name: GEMCITABINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AP
Application Number: A202485
Product Number: 002
Approval Date: May 7, 2013
Applicant Holder Full Name: JIANGSU HANSOH PHARMACEUTICAL GROUP CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information