Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International
02 1EUROAPI
03 1Transo-Pharm USA LLC
04 1LGM Pharma
05 3Bayer AG
06 2MSN Laboratories
07 1NEWCHEM SPA
08 1Yonsung Fine Chemicals
09 1Zhejiang Ausun Pharmaceutical
01 1China
02 1France
03 3Germany
04 2India
05 1Italy
06 1South Korea
07 1Taiwan
08 2U.S.A
01 4Active
02 2Inactive
03 6Blank
01 12Blank
01 12Blank
01 1WC-0349
02 1WC-0349A12
03 10Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33153
Submission : 2018-09-28
Status : Active
Type : II
NDC Package Code : 82231-109
Start Marketing Date : 2018-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF, CN |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-09-13
Pay. Date : 2021-07-09
DMF Number : 34695
Submission : 2020-03-31
Status : Active
Type : II
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm :
NDC Package Code : 54893-0017
Start Marketing Date : 2012-05-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36022
Submission : 2021-06-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17170
Submission : 2004-02-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9140
Submission : 1991-05-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11706
Submission : 1995-10-12
Status : Inactive
Type : II
Date of Issue : 2021-04-23
Valid Till : 2022-05-05
Written Confirmation Number : WC-0349A12
Address of the Firm :
NDC Package Code : 54893-0017
Start Marketing Date : 2012-05-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Iloprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iloprost, including repackagers and relabelers. The FDA regulates Iloprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iloprost 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 Iloprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iloprost supplier is an individual or a company that provides Iloprost active pharmaceutical ingredient (API) or Iloprost finished formulations upon request. The Iloprost suppliers may include Iloprost API manufacturers, exporters, distributors and traders.
click here to find a list of Iloprost suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 9 companies offering Iloprost
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