Axplora- The partner of choice for complex APIs.
01 1Axplora
02 2Evonik
03 1Suanfarma
04 1Advanced Accelerator Applications
05 2Ajinomoto Company
06 1Bajaj Healthcare
07 1Hangzhou Think Chemical Co.Ltd
08 1Kyowa Hakko Bio
09 1Mitsubishi Tanabe Pharma
10 2Pfizer Inc
11 1SAFC
12 1SHANGHAI KYOWA AMINO ACID CO., LTD.
13 1SIGMA TAU
14 1Salvi Chemical Industries
15 1Sichuan Tongsheng Amino Acid Co., Ltd
16 1Sigma-Aldrich Corporation
17 1Yangzhou Gami Biochem Co. Ltd
18 1Blank
01 3China
02 1France
03 3Germany
04 2India
05 5Japan
06 1Spain
07 5U.S.A
08 1Blank
01 3Active
02 7Inactive
03 11Blank
01 5Valid
02 16Blank
01 1223MF10042
02 1224MF10009
03 1225MF10189
04 1226MF10123
05 17Blank
01 21Blank
Certificate Number : R1-CEP 2003-057 - Rev 05
Issue Date : 2022-04-04
Type : Chemical
Substance Number : 930
Status : Valid
Registration Number : 226MF10123
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2014-06-18
Latest Date of Registration :
Registration Number : 225MF10189
Registrant's Address : 33, Rue de Verdun Ham, France
Initial Date of Registration : 2013-10-09
Latest Date of Registration :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17233
Submission : 2004-03-12
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-02-26
Pay. Date : 2021-02-23
DMF Number : 26280
Submission : 2012-08-02
Status : Active
Type : II
Certificate Number : R1-CEP 2012-249 - Rev 01
Issue Date : 2021-10-22
Type : Chemical
Substance Number : 930
Status : Valid
Registration Number : 223MF10042
Registrant's Address : No. 718, Rongle East Road, Songjiang District, Shanghai, People's Republic of China
Initial Date of Registration : 2011-03-10
Latest Date of Registration :
NDC Package Code : 17333-023
Start Marketing Date : 2002-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-08-27
Pay. Date : 2020-11-30
DMF Number : 31651
Submission : 2017-04-20
Status : Active
Type : II
Certificate Number : R1-CEP 1998-065 - Rev 02
Issue Date : 2013-12-20
Type : Chemical
Substance Number : 930
Status : Valid
NDC Package Code : 17333-023
Start Marketing Date : 2002-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3323
Submission : 1978-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31023
Submission : 2016-09-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1835
Submission : 1971-12-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 446
Submission : 1961-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2171
Submission : 1973-10-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12170
Submission : 1996-10-08
Status : Inactive
Type : II
Certificate Number : R1-CEP 1999-083 - Rev 04
Issue Date : 2022-04-27
Type : Chemical
Substance Number : 930
Status : Valid
Registration Number : 224MF10009
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2012-01-18
Latest Date of Registration :
NDC Package Code : 12497-1028
Start Marketing Date : 1978-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Certificate Number : R1-CEP 2012-007 - Rev 00
Issue Date : 2018-03-01
Type : Chemical
Substance Number : 930
Status : Valid
NDC Package Code : 74920-007
Start Marketing Date : 2020-03-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5095
Submission : 1983-10-12
Status : Inactive
Type : II
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A Lysine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysine Hydrochloride, including repackagers and relabelers. The FDA regulates Lysine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysine Hydrochloride 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 Lysine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lysine Hydrochloride supplier is an individual or a company that provides Lysine Hydrochloride active pharmaceutical ingredient (API) or Lysine Hydrochloride finished formulations upon request. The Lysine Hydrochloride suppliers may include Lysine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Lysine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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