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 1Jai Radhe Sales
08 1Century Pharmaceuticals
09 1HRV Global Life Sciences
10 1Capital Farma
11 1Ax Pharmaceutical Corporation
12 1Balaji Corporation
13 1Biopeptek Pharmaceuticals
14 1C-Squared Pharma
15 2CHEMO
16 1Ceyone Life Sciences
17 1Chemignition Laboratory
18 1Darmerica
19 1DongWha Pharm
20 1Dr Pradeep Reddy’s Laboratories Private Limited
21 1Everlight Chemical
22 1FDC
23 1Flax Laboratories
24 1Fleming Laboratories
25 1Globofarm International
26 1Guangdong Raffles PharmaTech Co Ltd
27 1Guangzhou Tosun Pharmaceutical
28 2Industriale Chimica
29 1Kyowa Pharma Chemical Co Ltd
30 2Laurus Labs
31 1Letco Medical
32 1Lupin Ltd
33 1MSN Laboratories
34 1Maprimed
35 1Medisca
36 1Monvi Labs
37 1NEWCHEM SPA
38 1Piramal Enterprises Limited
39 2ScinoPharm Taiwan Ltd
40 1Shenzhen HwaGen Pharmaceutical
41 1Tecoland Corporation
42 1Teva Pharmaceutical Industries
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44 1Yonsung Fine Chemicals
45 1Zhejiang Ausun Pharmaceutical
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05 2France
06 17India
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14 7U.S.A
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01 1220MF10035
02 1224MF10081
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04 1229MF10098
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01 1WC-0177
02 1WC-0177A
03 1WC-0229
04 1WC-0349
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01 150-1-ND
02 15242-1-ND
03 1767-1-ND
04 1Number 97-4-ND
05 1Su469-4-ND
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01 112079-1067
02 124002-0021
03 138779-3066
04 140016-005
05 142385-030
06 154245-7036
07 154893-0009
08 155545-0705
09 155679-113
10 157741-3000
11 161556-070
12 162991-3185
13 163190-0290
14 163190-0630
15 165035-130
16 165129-1206
17 168245-0004
18 171052-276
19 173212-076
20 173377-230
21 176397-016
22 182133-102
23 182231-102
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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.
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
Capital Farma, a leading European pharmaceutical company focusing on the development & distribution of niche APIs & Pharma Services.
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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 DURYSTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DURYSTA, including repackagers and relabelers. The FDA regulates DURYSTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DURYSTA 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 DURYSTA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DURYSTA supplier is an individual or a company that provides DURYSTA active pharmaceutical ingredient (API) or DURYSTA finished formulations upon request. The DURYSTA suppliers may include DURYSTA API manufacturers, exporters, distributors and traders.
click here to find a list of DURYSTA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 45 companies offering DURYSTA
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