Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 3Supriya Lifescience
02 1Naprod Life Sciences
03 2Advanz Pharma
04 3Aurobindo Pharma Limited
05 1Bharat Parenterals Limited
06 3Biological E
07 3ENDO OPERATIONS
08 1EUROVET ANIMAL HEALTH B.V.
09 4Farbe Firma
10 2Fresenius Kabi USA
11 3Fresenius SE & Co. KGaA
12 2GL Pharma
13 3GLAND PHARMA LIMITED
14 2Hikma Pharmaceuticals
15 2Hospira, Inc.
16 1Madras Pharmaceuticals
17 3Micro Healthcare
18 1Molteni Farmaceutici
19 1Myungmoon Pharm. Co., LTD.
20 8Pfizer Inc
21 3Quad Pharma
22 1R Key Enterprises
23 2SEARCHLIGHT PHARMA
24 1STERIMAX INC
25 2Sandoz B2B
26 2Umedica Laboratories
27 1VETOQUINOL N A INC
28 1Verve Human Care Laboratories
29 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania
01 6INJ
02 15INJECTABLE;INJECTION
03 3INJECTION
04 1Injectable
05 3Injectable; Injection
06 9Injection
07 1Injection
08 4Injection fluid, resolution
09 1Ketamine 100Mg 2Ml 5 Units Parenteral Use
10 1Liquid Injection
11 8SOLUTION
12 4SOLUTION FOR INJECTION
13 2Solution for Injection
14 2Solution for injection
15 3Vial
01 2Dossier Availability- Q2 2017
02 9Generic
03 8Narcotic (CDSA I)
04 15RX
05 29Blank
01 1ANESKETIN
02 5KETALAR
03 3KETAMINE HCL
04 12KETAMINE HYDROCHLORIDE
05 2KETAMINE HYDROCHLORIDE INJECTION USP
06 1KETAMINE INJECTION, BP
07 1KETASET
08 6Ketalar
09 2Ketamin Abcur
10 1Ketamine
11 1Ketamine 100mg/1ml Fresenius
12 1Ketamine 10mg/1ml Fresenius
13 1Ketamine 50mg/1ml Fresenius
14 2Ketanest-S
15 3Micro-Ketamine
16 1Mortorin
17 1NARKETAN
18 1VERKET
19 18Blank
01 2Austria
02 8Canada
03 17India
04 1Italy
05 6Norway
06 6South Africa
07 1South Korea
08 4Sweden
09 18USA
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
Naprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Liquid 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 : 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
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
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
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
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
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
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
Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/ML
Packaging :
Approval Date : 2023-01-24
Application Number : 216809
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : KETAMINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/ML
Packaging :
Approval Date : 2023-01-24
Application Number : 216809
Regulatory Info : RX
Registration Country : USA
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
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
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
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
Regulatory Info :
Registration Country : Italy
Brand Name : Ketamine
Dosage Form : Ketamine 100Mg 2Ml 5 Units Parenteral Use
Dosage Strength : 5 vials 2ml 50 mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : Mortorin
Dosage Form : INJECTION
Dosage Strength : 576.8MG/10ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info :
Registration Country : Sweden
Brand Name : Ketalar
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 50 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Ketalar
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 10 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Ketanest-S
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 25 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Ketanest-S
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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
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
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 : Generic
Registration Country : India
Brand Name :
Dosage Form : INJECTION
Dosage Strength : 10MG/ML
Packaging : 10ml ; 20ml vial
Approval Date :
Application Number : 76092
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : INJECTION
Dosage Strength : 50MG/ML
Packaging : 10ml ; 20ml vial
Approval Date :
Application Number : 74549
Regulatory Info : Generic
Registration Country : India
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
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