Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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01 1Seqens
02 1LGM Pharma
03 1PCAS
04 1Seqens CDMO
05 1Virupaksha Organics
06 2Supriya Lifescience
07 1Tenatra Exports
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09 2Arevipharma
10 1Ax Pharmaceutical Corporation
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01 1Algeria
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07 10India
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09 6U.S.A
10 3United Kingdom
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01 6Active
02 2Inactive
03 22Blank
01 6Valid
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01 1218MF10980
02 29Blank
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01 2WC-0218
02 1WC-0407
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04 1WC-0596
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01 110920-597
02 110920-701
03 138779-1754
04 149169-1041
05 149452-3912
06 151552-0697
07 151927-0120
08 151927-0292
09 154382-114
10 154382-128
11 160592-401
12 161281-8000
13 162991-1087
14 170600-035
15 173377-250
16 182393-116
17 14Blank
01 30Blank
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-11-05
Pay. Date : 2019-10-28
DMF Number : 7686
Submission : 1988-09-22
Status : Active
Type : II
Certificate Number : CEP 2005-281 - Rev 02
Issue Date : 2024-03-11
Type : Chemical
Substance Number : 1020
Status : Valid
Registration Number : 218MF10980
Registrant's Address : Raiffeisenstrasse 4, D-77933 Lahr Germany
Initial Date of Registration : 2006-12-01
Latest Date of Registration :
NDC Package Code : 54382-128
Start Marketing Date : 1989-08-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
| Available Reg Filing : ASMF, CA |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
NDC Package Code : 49169-1041
Start Marketing Date : 2024-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54382-114
Start Marketing Date : 1989-02-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-12-22
Pay. Date : 2022-12-20
DMF Number : 27921
Submission : 2014-01-15
Status : Active
Type : II
Certificate Number : CEP 2016-194 - Rev 01
Issue Date : 2024-05-07
Type : Chemical
Substance Number : 1020
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 : 61281-8000
Start Marketing Date : 2013-07-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37014
Submission : 2022-03-29
Status : Active
Type : II
Certificate Number : CEP 2022-157 - Rev 00
Issue Date : 2024-03-04
Type : Chemical
Substance Number : 1020
Status : Valid
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm :
NDC Package Code : 70600-035
Start Marketing Date : 2022-03-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF, BR |
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 : 5462
Submission : 1984-07-17
Status : Inactive
Type : II

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PharmaCompass offers a list of Ketamine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ketamine Hydrochloride manufacturer or Ketamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ketamine Hydrochloride manufacturer or Ketamine Hydrochloride supplier.
A Ketaset manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketaset, including repackagers and relabelers. The FDA regulates Ketaset manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketaset API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ketaset manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ketaset supplier is an individual or a company that provides Ketaset active pharmaceutical ingredient (API) or Ketaset finished formulations upon request. The Ketaset suppliers may include Ketaset API manufacturers, exporters, distributors and traders.
click here to find a list of Ketaset suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 27 companies offering Ketaset
Get in contact with the supplier of your choice: