EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 2Coral Drugs Private Limited
03 1Vamsi Labs
04 1Seqens
05 1Axplora
06 1Symbiotec Pharmalab
07 2Aarti Pharmalabs
08 1TAPI Technology & API Services
09 1Aurisco Pharmaceutical
10 1Balaji Corporation
11 1Beijing Breathgreen Healthcare
12 1CHEMO
13 1Cipla
14 1GSK
15 1Guangzhou Topwork Chemical
16 1Guangzhou Tosun Pharmaceutical
17 1Hovione
18 1Industriale Chimica
19 1Lupin Ltd
20 1Micro Orgo Chem
21 1NEWCHEM SPA
22 1Sterling Spa
23 1Sudarshan Pharma
24 1Teva Pharmaceutical Industries
01 4China
02 2France
03 1Germany
04 11India
05 2Israel
06 3Italy
07 1Portugal
08 1Spain
09 1United Kingdom
01 12Active
02 14Blank
01 4Valid
02 22Blank
01 1304MF10038
02 1305MF10120
03 24Blank
01 1WC-0009
02 1WC-0099
03 1WC-295
04 23Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32040
Submission : 2017-10-02
Status : Active
Type : II
Certificate Number : R0-CEP 2022-018 - Rev 00
Issue Date : 2023-03-06
Type : Chemical
Substance Number : 2768
Status : Valid
Date of Issue : 2022-09-16
Valid Till : 2025-07-05
Written Confirmation Number : WC-0009
Address of the Firm :
NDC Package Code : 49076-6451
Start Marketing Date : 2022-02-25
End Marketing Date : 2025-12-31
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.
NDC Package Code : 66412-0767
Start Marketing Date : 2023-09-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-29
Pay. Date : 2014-09-30
DMF Number : 28554
Submission : 2014-09-30
Status : Active
Type : II
Registration Number : 304MF10038
Registrant's Address : Offer Park, Building C, 4th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 4970602, Israel
Initial Date of Registration : 2022-02-17
Latest Date of Registration : --
NDC Package Code : 58175-0553
Start Marketing Date : 2009-03-25
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 : 40090
Submission : 2024-06-13
Status : Active
Type : II
Available Reg Filing : EU |
NDC Package Code : 22552-0042
Start Marketing Date : 2015-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33955
Submission : 2020-07-14
Status : Active
Type : II
Date of Issue : 2024-05-20
Valid Till : 2027-05-20
Written Confirmation Number : WC-295
Address of the Firm :
NDC Package Code : 15308-2021
Start Marketing Date : 2020-07-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2022-015 - Rev 01
Issue Date : 2024-03-11
Type : Chemical
Substance Number : 2768
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36316
Submission : 2021-10-22
Status : Active
Type : II
Certificate Number : R0-CEP 2021-372 - Rev 00
Issue Date : 2023-03-07
Type : Chemical
Substance Number : 2768
Status : Valid
NDC Package Code : 49076-6451
Start Marketing Date : 2022-02-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm :
NDC Package Code : 15308-2021
Start Marketing Date : 2020-07-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36621
Submission : 2023-12-24
Status : Active
Type : II
NDC Package Code : 47848-057
Start Marketing Date : 2018-10-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24647
Submission : 2011-02-18
Status : Active
Type : II
NDC Package Code : 64918-1915
Start Marketing Date : 2022-01-04
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 : 36736
Submission : 2022-02-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31713
Submission : 2017-05-31
Status : Active
Type : II
NDC Package Code : 50909-5171
Start Marketing Date : 2017-05-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-03-03
Pay. Date : 2021-01-22
DMF Number : 33636
Submission : 2019-03-21
Status : Active
Type : II
Certificate Number : CEP 2022-238 - Rev 00
Issue Date : 2023-09-07
Type : Chemical
Substance Number : 2768
Status : Valid
NDC Package Code : 16812-007
Start Marketing Date : 2023-07-31
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 : 37465
Submission : 2022-11-21
Status : Active
Type : II
NDC Package Code : 71586-006
Start Marketing Date : 2024-11-07
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 : 31938
Submission : 2017-09-08
Status : Active
Type : II
NDC Package Code : 52482-008
Start Marketing Date : 2014-06-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2008-05-07
Registration Number : 89-5-ND
Manufacturer Name : Glaxo Wellcome Manufacturing Pte Ltd@[Pulverization Process Manufacturing Company]Glaxo Operations UK Limited (trading as Glaxo Wellcome Operations)
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@[Micronization Process Manufacturer]Priory Street, Ware, Hertfordshire SG12 0DJ, UK
Registration Number : 305MF10120
Registrant's Address : Via E. H. Grieg, 13,21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2023-11-15
Latest Date of Registration : --
A Fluticasone Furoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluticasone Furoate, including repackagers and relabelers. The FDA regulates Fluticasone Furoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluticasone Furoate 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 Fluticasone Furoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluticasone Furoate supplier is an individual or a company that provides Fluticasone Furoate active pharmaceutical ingredient (API) or Fluticasone Furoate finished formulations upon request. The Fluticasone Furoate suppliers may include Fluticasone Furoate API manufacturers, exporters, distributors and traders.
click here to find a list of Fluticasone Furoate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 24 companies offering Fluticasone Furoate
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