KYTRIL
GRANISETRON HYDROCHLORIDE
Approval overview KYTRIL is listed in Drugs@FDA under application 020239 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient GRANISETRON HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ROCHE Submission history Latest submission status date: 2011-04-29 00:00:00.
Structured Monograph
Clinical summary
Approval overview KYTRIL is listed in Drugs@FDA under application 020239 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient GRANISETRON HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - EQ 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ROCHE Submission history Latest submission status date: 2011-04-29 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.