USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
01 1USV Private Limited
02 1TAPI Technology & API Services
03 1Ajinomoto Company
04 1Assia Chemical Industries Ltd
05 1Aurobindo Pharma Limited
06 2Cadila Pharmaceuticals
07 1Cipla
08 1Ind Swift Laboratories Limited
09 1Kyongbo Pharmaceutical Co., Ltd
10 1Teva Pharmaceutical Industries
11 2Unichem Laboratories Limited
12 1Zydus Lifesciences
01 9India
02 3Israel
03 1Japan
04 1South Korea
01 7Active
02 3Inactive
03 4Blank
01 1Valid
02 1Withdrawn by Holder
03 12Blank
01 1217MF10298
02 1222MF10186
03 1223MF10114
04 1224MF10051
05 10Blank
01 1WC-0003
02 1WC-0012
03 1WC-0062
04 1WC-0074
05 10Blank
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-17
Pay. Date : 2013-03-08
DMF Number : 26882
Submission : 2013-03-25
Status : Active
Type : II
Date of Issue : 2022-06-27
Valid Till : 2025-06-02
Written Confirmation Number : WC-0012
Address of the Firm :
NDC Package Code : 62147-0080
Start Marketing Date : 2009-12-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-08
Pay. Date : 2012-12-13
DMF Number : 17910
Submission : 2004-12-16
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-02-07
Pay. Date : 2013-07-19
DMF Number : 26518
Submission : 2013-06-21
Status : Active
Type : II
NDC Package Code : 65691-0083
Start Marketing Date : 2013-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21484
Submission : 2008-03-25
Status : Active
Type : II
Certificate Number : CEP 2015-134 - Rev 01
Issue Date : 2024-11-12
Type : Chemical
Substance Number : 2575
Status : Valid
Date of Issue : 2022-06-17
Valid Till : 2025-07-21
Written Confirmation Number : WC-0062
Address of the Firm :
NDC Package Code : 53747-020
Start Marketing Date : 2008-03-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-04-23
Pay. Date : 2014-12-31
DMF Number : 28934
Submission : 2015-01-05
Status : Active
Type : II
NDC Package Code : 53747-020
Start Marketing Date : 2008-03-25
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 : 37501
Submission : 2022-09-20
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-30
Pay. Date : 2012-12-21
DMF Number : 20231
Submission : 2007-01-27
Status : Active
Type : II
Date of Issue : 2022-06-03
Valid Till : 2025-05-27
Written Confirmation Number : WC-0003
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21962
Submission : 2008-09-09
Status : Inactive
Type : II
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074
Address of the Firm :
NDC Package Code : 65691-0083
Start Marketing Date : 2013-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11155
Submission : 1994-10-24
Status : Inactive
Type : II
Registration Number : 217MF10298
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-06-30
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17906
Submission : 2004-12-13
Status : Inactive
Type : II
Certificate Number : R0-CEP 2015-308 - Rev 00
Issue Date : 2017-06-08
Type : Chemical
Substance Number : 2575
Status : Withdrawn by Holder
NDC Package Code : 53104-7595
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Nateglinide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nateglinide, including repackagers and relabelers. The FDA regulates Nateglinide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nateglinide 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 Nateglinide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nateglinide supplier is an individual or a company that provides Nateglinide active pharmaceutical ingredient (API) or Nateglinide finished formulations upon request. The Nateglinide suppliers may include Nateglinide API manufacturers, exporters, distributors and traders.
click here to find a list of Nateglinide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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