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:
Application Number: A202063
Product Number: 001
Approval Date: Sep 11, 2012
Applicant Holder Full Name: EMCURE PHARMACEUTICALS LTD
Marketing Status:
Discontinued
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: No
TE Code:
Application Number: A202063
Product Number: 002
Approval Date: Sep 11, 2012
Applicant Holder Full Name: EMCURE PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information