General MedicationsINJECTIONGeneric
GEMCITABINE
GEMCITABINE
Standard Dose
200MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary
Approval overview GEMCITABINE is listed in Drugs@FDA under application 078460 (ANDA).
Marketing status: None (Tentative Approval) Active ingredient GEMCITABINE Form and strength INJECTABLE; INJECTION - 200MG Sponsor EUROHLTH INTL Submission history Latest submission status date: 2010-01-19 00:00:00.
Structured Monograph
Clinical summary
Approval overview GEMCITABINE is listed in Drugs@FDA under application 078460 (ANDA). Marketing status: None (Tentative Approval) Active ingredient GEMCITABINE Form and strength INJECTABLE; INJECTION - 200MG Sponsor EUROHLTH INTL Submission history Latest submission status date: 2010-01-19 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: None (Tentative Approval)
Interaction Notes
- No interaction notes stored yet.