EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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01 1EUROAPI
02 2Coral Drugs Private Limited
03 2Vamsi Labs
04 1Axplora
05 1Sanofi
06 1LGM Pharma
07 1Seqens
08 1Symbiotec Pharmalab
09 1Wavelength Pharmaceuticals
10 1Jai Radhe Sales
11 1Aarti Pharmalabs
12 1Century Pharmaceuticals
13 1Tenatra Exports
14 1TAPI Technology & API Services
15 1Swati Spentose
16 1Willow Birch Pharma
17 1Symbiotica Speciality Ingredients Sdn Bhd
18 1Curia
19 1ALPS Pharmaceutical Ind. Co. Ltd.
20 1Amphastar Pharmaceuticals
21 1Apotex Inc
22 1Apotex Pharmachem
23 1Aspire Lifesciences Pvt Ltd
24 2Aurisco Pharmaceutical
25 1Balaji Corporation
26 1Beijing Breathgreen Healthcare
27 2Breathgreen Pharmaceuticals
28 1CHEMO
29 1Chongqing Huapont Pharmaceutical
30 4Cipla
31 2GSK
32 1Grefuel
33 1Guangzhou Topwork Chemical
34 1Guangzhou Tosun Pharmaceutical
35 1Henan Lihua Pharmaceutical
36 1Hikma Pharmaceuticals
37 2Hovione
38 3Industriale Chimica
39 1Jayco Chemical Industries
40 1Letco Medical
41 1Lupin Ltd
42 1Mahima Life Sciences
43 1Maiden Group
44 1Medisca
45 1Micro Orgo Chem
46 1NEWCHEM SPA
47 1Natural Biogenex
48 1PRG Pharma
49 1Pcca
50 1Ravico Pharmaceutical
51 1ScinoPharm Taiwan Ltd
52 1Shandong Sito Bio-technology Co ltd
53 1Shouyuan Chemical
54 1Sicor de Mexico
55 4Sterling Spa
56 1Steroid SpA
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58 1Taro Pharmaceutical Industries
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60 1Tianjin Tianfa Pharmaceutical Import & Export
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14 8U.S.A
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01 27Active
02 4Inactive
03 47Blank
01 3Expired
02 25Valid
03 2Withdrawn by Holder
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01 1218MF10834
02 1222MF10142
03 1223MF10176
04 1224MF10093
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06 1303MF10172
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01 13923/25
02 1WC-0009
03 1WC-009
04 1WC-0099
05 1WC-0144
06 1WC-0155
07 1WC-0168
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01 120210325-209-J-917
02 120240531-209-J-1652
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01 115308-0200
02 116812-005
03 122552-0043
04 124002-0003
05 138779-2760
06 146439-8729
07 149076-5501
08 149867-0076
09 150909-5175
10 151927-0013
11 152221-106
12 152482-001
13 153104-7531
14 155018-301
15 158175-0361
16 159115-823
17 162756-223
18 162991-2698
19 163190-0440
20 163190-0500
21 163190-0520
22 163379-001
23 163592-0335
24 164918-1118
25 164918-1600
26 164918-1700
27 165089-0033
28 166412-0679
29 50Blank
01 78Blank
Certificate Number : R1-CEP 2018-040 - Rev 00
Issue Date : 2023-05-03
Type : Chemical
Substance Number : 1750
Status : Valid
Registration Number : 303MF10172
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2021-12-09
Latest Date of Registration :
Registrant Name : Mundipharma Korea Ltd.
Registration Date : 2024-05-31
Registration Number : 20240531-209-J-1652
Manufacturer Name : Euroapi France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-05-11
Pay. Date : 2018-04-10
DMF Number : 21879
Submission : 2008-08-12
Status : Active
Type : II
Certificate Number : R1-CEP 2005-055 - Rev 03
Issue Date : 2020-09-25
Type : Chemical
Substance Number : 1750
Status : Valid
Date of Issue : 2025-11-20
Valid Till : 2028-11-19
Written Confirmation Number : WC-0009
Address of the Firm :
NDC Package Code : 49076-5501
Start Marketing Date : 2018-10-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40285
Submission : 2024-08-13
Status : Inactive
Type : II
Certificate Number : CEP 2020-078 - Rev 03
Issue Date : 2025-06-24
Type : Chemical
Substance Number : 1750
Status : Valid
Date of Issue : 2025-11-12
Valid Till : 2028-07-02
Written Confirmation Number : WC-0155
Address of the Firm :
NDC Package Code : 66412-0679
Start Marketing Date : 2023-09-25
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-11-02
Pay. Date : 2018-10-31
DMF Number : 20463
Submission : 2007-04-24
Status : Active
Type : II
Certificate Number : CEP 2008-117 - Rev 02
Issue Date : 2024-05-23
Type : Chemical
Substance Number : 1750
Status : Valid
NDC Package Code : 46439-8729
Start Marketing Date : 2007-04-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R0-CEP 2013-158 - Rev 02
Issue Date : 2016-07-08
Type : Chemical
Substance Number : 1750
Status : Expired
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-23
Pay. Date : 2014-05-05
DMF Number : 15456
Submission : 2001-05-24
Status : Active
Type : II
Certificate Number : CEP 2007-192 - Rev 09
Issue Date : 2024-11-26
Type : Chemical
Substance Number : 1750
Status : Valid
Registration Number : 218MF10834
Registrant's Address : Ofer Park, Building E, 5th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 4970602, Israel
Initial Date of Registration : 2006-10-20
Latest Date of Registration :
| Available Reg Filing : ASMF |
NDC Package Code : 22552-0043
Start Marketing Date : 2015-01-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58175-0361
Start Marketing Date : 2000-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Fluticasone Propionate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Fluticasone Propionate manufacturer or Fluticasone Propionate supplier for your needs.
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A Flixotide Inhaler manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flixotide Inhaler, including repackagers and relabelers. The FDA regulates Flixotide Inhaler manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flixotide Inhaler 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 Flixotide Inhaler manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flixotide Inhaler supplier is an individual or a company that provides Flixotide Inhaler active pharmaceutical ingredient (API) or Flixotide Inhaler finished formulations upon request. The Flixotide Inhaler suppliers may include Flixotide Inhaler API manufacturers, exporters, distributors and traders.
click here to find a list of Flixotide Inhaler suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 64 companies offering Flixotide Inhaler
Get in contact with the supplier of your choice: