Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

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01 3Supriya Lifescience
02 2Abcur AB
03 2Abcur Ab
04 2Alfasan Netherlands BV
05 3Aurobindo Pharma Limited
06 1Baxter Healthcare Corporation
07 1Bela-Pharm GmbH & Co. KG
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33 1VETOQUINOL N A INC
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35 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania
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01 17INJECTABLE;INJECTION
02 3INJECTION
03 1Injectable
04 7Injectable Solution
05 3Injectable; Injection
06 12Injection
07 1Injection
08 1Ketamine 100Mg 2Ml 5 Units Parenteral Use
09 1Liquid Injection
10 8SOLUTION
11 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
12 9Solution For Injection
13 2Solution for Injection
14 3Vial
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01 4Approved
02 1Authorised
03 1Authorized
04 2Deregistered
05 2Dossier Availability- Q2 2017
06 3Generic
07 7Marketed
08 8NARCOTICS (CDSA I)
09 1Not Marketed
10 18RX
11 22Blank
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01 1ANESKETIN
02 1Belatamin vet.
03 5KETALAR
04 3KETAMINE HCL
05 15KETAMINE HYDROCHLORIDE
06 2KETAMINE HYDROCHLORIDE INJECTION USP
07 1KETAMINE INJECTION, BP
08 1KETASET
09 4Ketalar
10 2Ketamin Abcur
11 1Ketamine
12 2Ketamine Abcur
13 1Ketamine Le vet
14 1Ketamine Renaudin
15 2Ketanest-S
16 2Ketexx Vet
17 1Ketmin 10
18 1Ketmin 2 Vial
19 1Ketmin 5
20 1Ketolar
21 1Mortorin
22 1NARKETAN
23 1VERKET
24 18Blank
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01 2Austria
02 8Canada
03 20India
04 1Italy
05 1Malta
06 8Norway
07 1South Korea
08 1Spain
09 6Sweden
10 21USA
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 50MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 100MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 2008-09-30
Application Number : 76092
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 2001-12-28
Application Number : 76092
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 2002-10-25
Application Number : 76092
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 2023-01-13
Application Number : 215808
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 2023-01-13
Application Number : 215808
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 2025-04-18
Application Number : 215808
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 2023-01-24
Application Number : 216809
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 1996-03-22
Application Number : 74524
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 1996-03-22
Application Number : 74524
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 1996-06-27
Application Number : 74549
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 1996-06-27
Application Number : 74549
Regulatory Info : RX
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : KETAMINE HCL
Dosage Form : Injectable; Injection
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date :
Application Number : 71949
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : KETAMINE HCL
Dosage Form : Injectable; Injection
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date :
Application Number : 71950
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : KETAMINE HCL
Dosage Form : Injectable; Injection
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date :
Application Number : 71951
Regulatory Info :
Registration Country : USA

Regulatory Info : RX
Registration Country : USA
Brand Name : KETALAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 16812
Regulatory Info : RX
Registration Country : USA

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : KETALAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 16812
Regulatory Info : RX
Registration Country : USA

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : KETALAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 16812
Regulatory Info : RX
Registration Country : USA

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF