Visitor Monitoring Drug Details: KYTRIL
 
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Drug Details

Drug Name: KYTRIL
FDA Application No: (NDA) 020239
Active Ingredient(s): GRANISETRON HYDROCHLORIDE
Company: ROCHE
Original Approval or Tentative Approval Date: December 29, 1993
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
KYTRIL GRANISETRON HYDROCHLORIDEEQ 3MG BASE/MLINJECTABLE; INJECTION Discontinued No None
KYTRIL GRANISETRON HYDROCHLORIDEEQ 4MG BASE/4ML (EQ 1MG BASE/ML)INJECTABLE; INJECTION Prescription Yes None
KYTRIL GRANISETRON HYDROCHLORIDEEQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)INJECTABLE; INJECTION Prescription Yes None
KYTRIL GRANISETRON HYDROCHLORIDEEQ 1MG BASE/ML (EQ 1MG BASE/ML)INJECTABLE; INJECTION Prescription Yes None


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