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: A206617
Product Number: 001
Approval Date: Jun 25, 2021
Applicant Holder Full Name: HIKMA INTERNATIONAL PHARMACEUTICALS LLC
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: No
TE Code: AP
Application Number: A206617
Product Number: 002
Approval Date: Jun 25, 2021
Applicant Holder Full Name: HIKMA INTERNATIONAL PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information