DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 3DR REDDYS
02 1AM REGENT
03 3AMNEAL
04 1APOTEX INC
05 1AUROBINDO PHARMA USA
06 1BARR
07 3BAXTER HLTHCARE CORP
08 3BIONPHARMA
09 1CHARTWELL MOLECULAR
10 1DR REDDYS LABS LTD
11 2EPIC PHARMA LLC
12 2EUGIA PHARMA
13 3FRESENIUS KABI USA
14 5HIKMA
15 2HIKMA FARMACEUTICA
16 1INTRA SANA LABS
17 4MYLAN ASI
18 1NATCO PHARMA
19 3NORVIUM BIOSCIENCE
20 1ORBION PHARMS
21 2RISING
22 7ROCHE
23 4SANDOZ
24 2SANDOZ INC
25 1TARO
26 1TEVA PHARMS
27 1TEVA PHARMS USA
28 3WOCKHARDT USA
29 3YUNG SHIN PHARM
01 1INJECTABLE; INJECTION
02 50INJECTABLE;INJECTION
03 2SOLUTION;ORAL
04 13TABLET;ORAL
01 32DISCN
02 33RX
03 1Blank
01 55GRANISETRON HYDROCHLORIDE
02 3GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE
03 1GRANISOL
04 7KYTRIL
01 58No
02 7Yes
03 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Approval Date : 2007-12-31
Application Number : 77165
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AP
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Approval Date : 2008-06-30
Application Number : 77297
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AP
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
Approval Date : 2007-12-31
Application Number : 78392
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-29
Application Number : 20239
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1994-03-11
Application Number : 20239
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2004-09-17
Application Number : 20239
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1994-03-11
Application Number : 20239
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons**
Approval Date : 1995-03-16
Application Number : 20305
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons**
Approval Date : 1998-06-15
Application Number : 20305
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KYTRIL
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 2MG BASE/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2001-06-27
Application Number : 21238
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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