Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
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01 1Cayman Pharma s.r.o
02 1Gentec Pharmaceutical Group
03 1Chirogate International
04 2EUROAPI
05 1Transo-Pharm USA LLC
06 1LGM Pharma
07 1Veranova
08 1Jai Radhe Sales
09 1Century Pharmaceuticals
10 1HRV Global Life Sciences
11 1Capital Farma
12 1Balaji Corporation
13 1C-Squared Pharma
14 2CHEMO
15 1Ceyone Life Sciences
16 1Chemignition Laboratory
17 1DongWha Pharm
18 1Dr Pradeep Reddy’s Laboratories Private Limited
19 1Everlight Chemical
20 1FDC
21 1Fleming Laboratories
22 1Globofarm International
23 1Guangdong Raffles PharmaTech Co Ltd
24 1Guangzhou Tosun Pharmaceutical
25 1Industriale Chimica
26 1Kyowa Pharma Chemical Co Ltd
27 2Laurus Labs
28 1Lupin Ltd
29 1MSN Laboratories
30 1Monvi Labs
31 1NEWCHEM SPA
32 1Piramal Enterprises Limited
33 1ScinoPharm Taiwan, Ltd
34 1Shenzhen HwaGen Pharmaceutical
35 1Tecoland Corporation
36 1Teva Pharmaceutical Industries
37 1Tianwei Biotech Group
38 1Yonsung Fine Chemicals
39 1Zhejiang Ausun Pharmaceutical
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01 5China
02 1Czech Republic
03 2France
04 16India
05 1Ireland
06 1Israel
07 2Italy
08 1Japan
09 2South Korea
10 4Spain
11 3Taiwan
12 4U.S.A
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01 13Active
02 1Inactive
03 28Blank
01 42Blank
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01 1220MF10035
02 1224MF10081
03 1228MF10186
04 1229MF10098
05 1229MF10152
06 1229MF10165
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01 1WC-0177
02 1WC-0177A
03 1WC-0229
04 1WC-0349
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GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-12
Pay. Date : 2013-02-11
DMF Number : 24353
Submission : 2011-01-10
Status : Active
Type : II
NDC Package Code : 61556-070
Start Marketing Date : 2015-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Eltek Pharmachem Co., Ltd.
Registration Date : 2021-11-23
Registration Number : Su469-4-ND
Manufacturer Name : Cayman Pharma sro
Manufacturer Address : Ul. Práce 657, 277 11 Neratovice, Czech Republic
Available Reg Filing : CA, |
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21382
Submission : 2008-02-26
Status : Active
Type : II
NDC Package Code : 68245-0004
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-05-20
Pay. Date : 2015-12-08
DMF Number : 29560
Submission : 2015-07-17
Status : Active
Type : II
Registration Number : 229MF10098
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2017-05-24
Latest Date of Registration :
NDC Package Code : 82231-102
Start Marketing Date : 2018-03-07
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 : N/A
Rev. Date :
Pay. Date :
DMF Number : 20911
Submission : 2007-10-04
Status : Active
Type : II
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
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PharmaCompass offers a list of Bimatoprost API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Bimatoprost manufacturer or Bimatoprost supplier for your needs.
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PharmaCompass also assists you with knowing the Bimatoprost API Price utilized in the formulation of products. Bimatoprost API Price is not always fixed or binding as the Bimatoprost Price is obtained through a variety of data sources. The Bimatoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bimatoprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bimatoprost, including repackagers and relabelers. The FDA regulates Bimatoprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bimatoprost 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 Bimatoprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bimatoprost supplier is an individual or a company that provides Bimatoprost active pharmaceutical ingredient (API) or Bimatoprost finished formulations upon request. The Bimatoprost suppliers may include Bimatoprost API manufacturers, exporters, distributors and traders.
click here to find a list of Bimatoprost suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 39 companies offering Bimatoprost
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