Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International
02 1EUROAPI
03 1LGM Pharma
04 1Aspen Biopharma Labs
05 1DongWha Pharm
06 1Guangzhou Tosun Pharmaceutical
07 1Kyowa Pharma Chemical Co Ltd
08 1Pfizer Inc
09 1Shenzhen HwaGen Pharmaceutical
10 1Yonsung Fine Chemicals
11 1Zhejiang Ausun Pharmaceutical
01 3China
02 1France
03 1India
04 1Japan
05 2South Korea
06 1Taiwan
07 2U.S.A
01 4Active
02 7Blank
01 1Valid
02 10Blank
01 1230MF10070
02 1230MF10136
03 9Blank
01 11Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37975
Submission : 2023-04-26
Status : Active
Type : II
NDC Package Code : 68245-0015
Start Marketing Date : 2018-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11563
Submission : 1995-07-06
Status : Active
Type : II
Registration Number : 230MF10136
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2018-09-21
Latest Date of Registration : --
NDC Package Code : 82231-104
Start Marketing Date : 2014-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Ferring Pharmaceutical Co., Ltd.
Registration Date : 2022-11-02
Registration Number : 20221102-209-J-1396
Manufacturer Name : EUROAPI Hungary Ltd.
Manufacturer Address : To u. 1-5., Budapest, 1045, Hungary
Available Reg Filing : ASMF |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5202
Submission : 1984-01-03
Status : Active
Type : II
NDC Package Code : 0009-0058
Start Marketing Date : 2015-08-26
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 : 11274
Submission : 1994-12-27
Status : Active
Type : II
Certificate Number : R1-CEP 2003-029 - Rev 02
Issue Date : 2022-08-09
Type : Chemical
Substance Number : 1311
Status : Valid
Registration Number : 230MF10070
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2018-06-07
Latest Date of Registration : --
NDC Package Code : 12079-0485
Start Marketing Date : 2010-11-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 40016-012
Start Marketing Date : 2021-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Dinoprostone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dinoprostone, including repackagers and relabelers. The FDA regulates Dinoprostone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dinoprostone 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 Dinoprostone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dinoprostone supplier is an individual or a company that provides Dinoprostone active pharmaceutical ingredient (API) or Dinoprostone finished formulations upon request. The Dinoprostone suppliers may include Dinoprostone API manufacturers, exporters, distributors and traders.
click here to find a list of Dinoprostone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 11 companies offering Dinoprostone
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