Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 2Pfizer CentreOne
02 1Coral Drugs Private Limited
03 2Axplora
04 1LGM Pharma
05 1Symbiotec Pharmalab
06 1TAPI Technology & API Services
07 1Bayer AG
08 2Fujifilm Diosynth Biotechnologies
09 1GSK
10 1Hanways Chempharm
11 1JIANGSU GRAND XIANLE PHARMACEUTICAL CO LTD
12 1Merck & Co
13 1Pfizer Inc
14 1SIMS Srl
15 1Taizhou Taifa Pharmaceuticals Co. Ltd.
16 1Teva Pharmaceutical Industries
17 1Zhejiang Xianju Pharmaceutical Co. Ltd
18 1Zhejiang Xianju Yangguang Bioproducts
19 1Blank
01 5China
02 3Germany
03 2India
04 2Israel
05 1Italy
06 5U.S.A
07 3United Kingdom
08 1Blank
01 7Active
02 7Inactive
03 8Blank
01 8Valid
02 14Blank
01 22Blank
01 22Blank
Certificate Number : R1-CEP 2006-230 - Rev 01
Issue Date : 2014-04-23
Type : Chemical
Substance Number : 1593
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-03-25
Pay. Date : 2021-03-22
DMF Number : 12662
Submission : 1997-09-20
Status : Active
Type : II
Certificate Number : CEP 2002-181 - Rev 09
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 1593
Status : Valid
NDC Package Code : 46439-8722
Start Marketing Date : 1998-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-04-09
Registration Number : 20210409-211-J-738
Manufacturer Name : Farmabios SpA@Micro-Macinazione SA@IMS srl@Micro-Macinazione SA
Manufacturer Address : Via Pavia 1-27027 Gropello Cairoli (PV), Italy@Zona Artigianale 11, 6995 Madonna del Piano, Switzerland@Via Venezia Giulia 23, 20157 Milano@Via Cantonale 4, 6998 Monteggio, Switzerland
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-29
Pay. Date : 2012-11-09
DMF Number : 12687
Submission : 1997-10-08
Status : Active
Type : II
Available Reg Filing : ASMF |
Certificate Number : R1-CEP 2008-020 - Rev 01
Issue Date : 2014-09-04
Type : Chemical
Substance Number : 1593
Status : Valid
Certificate Number : R1-CEP 2002-154 - Rev 05
Issue Date : 2019-02-11
Type : Chemical
Substance Number : 1593
Status : Valid
NDC Package Code : 46439-8722
Start Marketing Date : 1998-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-04-09
Registration Number : 20210409-211-J-738
Manufacturer Name : Farmabios SpA@Micro-Macinazione SA@IMS srl@Micro-Macinazione SA
Manufacturer Address : Via Pavia 1-27027 Gropello Cairoli (PV), Italy@Zona Artigianale 11, 6995 Madonna del Piano, Switzerland@Via Venezia Giulia 23, 20157 Milano@Via Cantonale 4, 6998 Monteggio, Switzerland
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-01-26
Pay. Date : 2023-11-07
DMF Number : 24592
Submission : 2011-01-31
Status : Active
Type : II
Certificate Number : CEP 2012-010 - Rev 04
Issue Date : 2024-11-19
Type : Chemical
Substance Number : 1593
Status : Valid
NDC Package Code : 60722-1009
Start Marketing Date : 2023-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2020-03-03
Registration Number : 20200303-211-J-361
Manufacturer Name : Zhejiang Xianju Pharmaceutical Co., Ltd
Manufacturer Address : No.3 Donghai Fourth Avenue, Zhejiang Toumen Port Economic Development Zone, Linhai, Taizhou, Zhejiang, China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35601
Submission : 2021-01-29
Status : Active
Type : II
Certificate Number : R0-CEP 2020-293 - Rev 00
Issue Date : 2022-02-18
Type : Chemical
Substance Number : 1593
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-03-31
Pay. Date : 2014-10-31
DMF Number : 24583
Submission : 2011-01-26
Status : Active
Type : II
Certificate Number : R1-CEP 2012-011 - Rev 00
Issue Date : 2018-11-09
Type : Chemical
Substance Number : 1593
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27596
Submission : 2013-11-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1817
Submission : 1971-11-21
Status : Active
Type : II
NDC Package Code : 0009-5030
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Bansen Co., Ltd.
Registration Date : 2022-11-14
Registration Number : 20221114-211-J-1329
Manufacturer Name : Pharmacia & Upjohn Company LLC
Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001 USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6673
Submission : 1986-11-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12157
Submission : 1996-10-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2494
Submission : 1975-07-23
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3869
Submission : 1980-06-13
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7012
Submission : 1987-06-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5296
Submission : 1984-03-15
Status : Inactive
Type : II
Certificate Number : R1-CEP 2009-086 - Rev 01
Issue Date : 2021-12-17
Type : Chemical
Substance Number : 1593
Status : Valid
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1738
Submission : 1971-06-10
Status : Inactive
Type : II
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A Megace, Megace ES, Megestrol Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Megace, Megace ES, Megestrol Acetate, including repackagers and relabelers. The FDA regulates Megace, Megace ES, Megestrol Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Megace, Megace ES, Megestrol Acetate 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 Megace, Megace ES, Megestrol Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Megace, Megace ES, Megestrol Acetate supplier is an individual or a company that provides Megace, Megace ES, Megestrol Acetate active pharmaceutical ingredient (API) or Megace, Megace ES, Megestrol Acetate finished formulations upon request. The Megace, Megace ES, Megestrol Acetate suppliers may include Megace, Megace ES, Megestrol Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Megace, Megace ES, Megestrol Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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