 TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
 
										

 
				
									 
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01 1Transo-Pharm USA LLC
02 1Seqens
03 1Supriya Lifescience
04 1Maithri Drugs
05 1Alkem Laboratories
06 1Arevipharma
07 1Johnson & Johnson Innovative Medicine
08 1MSN Laboratories
09 1Nortec Quimica
									 
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01 1Brazil
02 1France
03 1Germany
04 4India
05 2U.S.A
									 
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01 6Active
02 3Blank
01 4Valid
02 5Blank
									 
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01 9Blank
									 
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01 1WC-0218
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01 9Blank
									 
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01 110920-700
02 154382-123
03 159014-0020
04 161281-8300
05 165267-117
06 170600-036
07 3Blank
01 9Blank
 Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16737
Submission : 2003-07-31
Status : Active
Type : II
Certificate Number : CEP 2017-216 - Rev 02
Issue Date : 2023-11-08
Type : Chemical
Substance Number : 1742
Status : Valid
NDC Package Code : 54382-123
Start Marketing Date : 2001-07-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF, BR, CA | 
 Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36426
Submission : 2021-11-08
Status : Active
Type : II
Certificate Number : CEP 2018-198 - Rev 01
Issue Date : 2025-01-31
Type : Chemical
Substance Number : 1742
Status : Valid
Date of Issue : 2025-09-02
Valid Till : 2028-07-02
Written Confirmation Number : WC-0218
Address of the Firm :
NDC Package Code : 61281-8300
Start Marketing Date : 2015-06-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF | 
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37012
Submission : 2022-08-04
Status : Active
Type : II
Certificate Number : CEP 2022-319 - Rev 00
Issue Date : 2024-05-03
Type : Chemical
Substance Number : 1742
Status : Valid
| Available Reg Filing : BR | 
 
											 
												GDUFA
DMF Review : Reviewed
Rev. Date : 2023-02-22
Pay. Date : 2023-01-31
DMF Number : 37647
Submission : 2022-12-09
Status : Active
Type : II
NDC Package Code : 59014-0020
Start Marketing Date : 2022-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT

 
											 
												GDUFA
DMF Review : Reviewed
Rev. Date : 2022-10-25
Pay. Date : 2022-10-14
DMF Number : 37461
Submission : 2022-09-26
Status : Active
Type : II

 
											 
												GDUFA
DMF Review : Reviewed
Rev. Date : 2023-01-30
Pay. Date : 2022-12-01
DMF Number : 36990
Submission : 2022-11-04
Status : Active
Type : II
Certificate Number : CEP 2022-404 - Rev 01
Issue Date : 2025-07-22
Type : Chemical
Substance Number : 1742
Status : Valid
NDC Package Code : 10920-700
Start Marketing Date : 2022-01-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

 
											 
												NDC Package Code : 70600-036
Start Marketing Date : 2022-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

 
											 
												NDC Package Code : 65267-117
Start Marketing Date : 2019-03-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

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PharmaCompass offers a list of Esketamine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Esketamine Hydrochloride manufacturer or Esketamine Hydrochloride supplier for your needs.
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A (-)-Ketamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (-)-Ketamine, including repackagers and relabelers. The FDA regulates (-)-Ketamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (-)-Ketamine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A (-)-Ketamine supplier is an individual or a company that provides (-)-Ketamine active pharmaceutical ingredient (API) or (-)-Ketamine finished formulations upon request. The (-)-Ketamine suppliers may include (-)-Ketamine API manufacturers, exporters, distributors and traders.
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We have 9 companies offering (-)-Ketamine
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