Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
01 1Omgene Life Sciences Pvt. Ltd
02 1ChemWerth Inc
03 1ANHUI ANKE BIOTECHNOLOGY (GROUP) CO., LTD
04 1BCN Peptides
05 1Chinese Peptide Company
06 1Hanways Chempharm
07 1Hybio Pharmaceutical
08 1Kaliberr Labs
09 1Piramal Pharma Solutions
10 2PolyPeptide Group
11 1Shenzhen JYMed Technology
12 1Smaart Pharmaceutticals
13 1Sun Pharmaceutical Industries Limited
14 1Tecoland Corporation
15 2Blank
01 5China
02 4India
03 1Spain
04 2Switzerland
05 3U.S.A
06 2Blank
01 2Active
02 2Inactive
03 13Blank
01 4Valid
02 13Blank
01 17Blank
01 1WC-0159
02 1WC-0237
03 15Blank
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34391
Submission : 2019-12-06
Status : Active
Type : II
NDC Package Code : 63586-0124
Start Marketing Date : 2019-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4g/4g)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Ferring Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-59-A-113-01
Manufacturer Name : PolyPeptide Laboratories (Sweden) AB
Manufacturer Address : Hogerudsgatan 21 SE-216 13 Limhamn
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25589
Submission : 2011-12-21
Status : Inactive
Type : II
Certificate Number : R0-CEP 2019-316 - Rev 00
Issue Date : 2021-05-21
Type : Chemical
Substance Number : 2646
Status : Valid
NDC Package Code : 63586-0124
Start Marketing Date : 2019-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4g/4g)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Ferring Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-59-A-113-01
Manufacturer Name : PolyPeptide Laboratories (Sweden) AB
Manufacturer Address : Hogerudsgatan 21 SE-216 13 Limhamn
Certificate Number : R0-CEP 2020-319 - Rev 00
Issue Date : 2021-10-28
Type : Chemical
Substance Number : 2646
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm :
Certificate Number : R0-CEP 2020-111 - Rev 00
Issue Date : 2022-05-23
Type : Chemical
Substance Number : 2646
Status : Valid
Certificate Number : R0-CEP 2021-470 - Rev 00
Issue Date : 2022-12-06
Type : Chemical
Substance Number : 2646
Status : Valid
Date of Issue : 2019-09-03
Valid Till : 2022-09-02
Written Confirmation Number : WC-0237
Address of the Firm :
NDC Package Code : 41701-009
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2014-07-25
Registration Number : 20140725-59-A-289-04
Manufacturer Name : Hemmo Pharmaceuticals Pvt. Ltd.
Manufacturer Address : C-43, MIDC, TTC Industrial Area, Turbhe, Off Thane Belapur Road, Dist. Thane-400613, India
Registrant Name : Hanlim Pharmaceutical Co., Ltd.
Registration Date : 2006-05-03
Registration Number : 20060503-59-A-191-03
Manufacturer Name : BCN Peptides SA
Manufacturer Address : Poligono Industrial Els Vinyets-Els Fogars, Sector Ⅱ-08777, Sant Quintide Mediona- Barcelona, Spain
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 : 39987
Submission : 2024-05-29
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 9995
Submission : 1992-12-10
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Terlipressin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terlipressin, including repackagers and relabelers. The FDA regulates Terlipressin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terlipressin 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 Terlipressin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terlipressin supplier is an individual or a company that provides Terlipressin active pharmaceutical ingredient (API) or Terlipressin finished formulations upon request. The Terlipressin suppliers may include Terlipressin API manufacturers, exporters, distributors and traders.
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