DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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01 3Dr. Reddy's Laboratories
02 3ATNAHS PHARMA UK LIMITED
03 2Adcock Ingram
04 3Altan Pharma
05 1American Regent
06 3Amneal Pharmaceuticals
07 2Apotex Inc
08 3Aurobindo Pharma Limited
09 1Aurovitas Spain, Sau
10 1Barr Laboratories
11 3Baxter Healthcare Corporation
12 3Bionpharma
13 1Chartwell Pharmaceuticals llc
14 2Epic Pharma. LLC.
15 7F. Hoffmann-La Roche
16 4Farbe Firma
17 2Flagship Biotech International Pvt. Ltd
18 1Fresenius Kabi AB Brunna
19 3Fresenius Kabi USA
20 1Ha Noi CPC1 Pharmaceutical JSC
21 1Hameln Pharma GmbH
22 7Hikma Pharmaceuticals
23 1Igenius Life Sciences
24 2Intra-Sana Laboratories
25 1LABORATORIOS NORMON SA
26 2Natco Pharma
27 1Natco Pharma (Canada) Inc
28 1Omega Laboratories Limited
29 1OrBion Pharmaceuticals
30 3PHARMOBEDIENT
31 2Pluviaendo
32 2Rising Pharmaceuticals Inc
33 2STADA Arzneimittel
34 6Sandoz B2B
35 1Taro Pharmaceutical Industries
36 2Teva Pharmaceutical Industries
37 4Viatris
38 3Wockhardt
39 1XYZ Pharma
40 1Yangtze River Pharmaceutical Group
41 3Yung Shin Pharm Industrial
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01 2Ampoule
02 1Concentrate For Injectable Solution
03 1Concentrate For Solution For Infusion
04 5Film Coated Tablet
05 2INJ
06 1INJECTABLE; INJECTION
07 50INJECTABLE;INJECTION
08 4Injectable Solution
09 8Injection
10 1LIQUID
11 3SOLUTION;ORAL
12 1Solution For Perfusion
13 1Solution for Injection
14 2TABLET
15 13TABLET;ORAL
16 1Tablet
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01 7Authorized
02 1Cancelled
03 34DISCN
04 4Generic
05 7Prescription
06 32RX
07 1Suspended
08 10Blank
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01 1APO-GRANISETRON
02 1Adco Granisetron 1 Mg/1 Ml
03 1Adco Granisetron 3 Mg/3 Ml
04 1BFS-Grani
05 56GRANISETRON HYDROCHLORIDE
06 1GRANISETRON HYDROCHLORIDE INJECTION
07 3GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE
08 1GRANISOL
09 3Granisetron Altan
10 1Granisetron Aurovitas Spain
11 1Granisetron Kabi
12 1Granisetron Normon
13 1Granisetron "Hameln"
14 2Granisetron "Stada"
15 7KYTRIL
16 3Kytril
17 2NAT-GRANISETRON
18 10Blank
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01 4Canada
02 1China
03 3Denmark
04 7India
05 2South Africa
06 9Spain
07 2Turkey
08 67USA
09 1Vietnam
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2007-12-31
Application Number : 77165
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-06-30
Application Number : 77297
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
Packaging :
Approval Date : 2007-12-31
Application Number : 78392
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2008-02-27
Application Number : 78037
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1993-12-29
Application Number : 20239
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1994-03-11
Application Number : 20239
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 2004-09-17
Application Number : 20239
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1994-03-11
Application Number : 20239
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1995-03-16
Application Number : 20305
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1998-06-15
Application Number : 20305
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 2001-06-27
Application Number : 21238
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-06-30
Application Number : 78090
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-06-30
Application Number : 78096
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2007-12-31
Application Number : 77177
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-06-30
Application Number : 77186
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-06-30
Application Number : 77187
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2007-12-31
Application Number : 77842
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
Packaging :
Approval Date : 2008-06-26
Application Number : 77913
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2008-01-03
Application Number : 77963
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : GRANISETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2007-12-31
Application Number : 78080
Regulatory Info : DISCN
Registration Country : USA
