Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 3Symbiotec Pharmalab
02 1Gonane Pharma
03 1Axplora
04 3EUROAPI
05 1Farmabios SPA
06 1Transo-Pharm USA LLC
07 1Aspen API
08 1Atman Pharma Private Limited
09 1TAPI Technology & API Services
10 1Anuh Pharma LTD
11 1Arudavis Labs
12 1Aurisco Pharmaceutical
13 2Bayer AG
14 1Biotechnica DWC
15 3Fujifilm Diosynth Biotechnologies
16 3Henan Lihua Pharmaceutical
17 1Hengdian Group
18 1Hubei Gedian Humanwell Pharmaceutical
19 1Hunan Yuxin Pharmaceutical
20 1JIANGSU GRAND XIANLE PHARMACEUTICAL CO LTD
21 1Laboratorio Syntex S.A
22 1Mahima Life Sciences
23 1Medimpex
24 1NEWCHEM SPA
25 1Nanjing Dorra Pharmaceutical Technology Co.,Ltd
26 1Otto Brandes
27 2Pfizer Inc
28 1Qingdao Qingmei Biotech
29 1Roussel Delma Pharmaceuticals
30 2Shandong Xinhua Pharmaceutical
31 1Steroid SpA
32 2Symbiotica Specialty Ingredients
33 1Tianjin Pharmaceutical Holdings Ltd
34 2Tianjin Tianyao Pharmaceuticals Co., Ltd.
35 1Unimax Group
36 2Zhejiang Xianju Pharmaceutical Co. Ltd
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01 1Algeria
02 1Argentina
03 17China
04 3France
05 5Germany
06 9India
07 1Israel
08 2Italy
09 2Malaysia
10 1Netherlands
11 4U.S.A
12 4United Kingdom
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01 12Active
02 10Inactive
03 28Blank
01 2Expired
02 12Valid
03 1Withdrawn by Holder
04 35Blank
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01 1218MF10379
02 1223MF10037
03 1227MF10238
04 1228MF10093
05 1302MF10041
06 1306MF10069
07 44Blank
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01 1WC-0161A2
02 2WC-0162A2
03 47Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24630
Submission : 2011-02-11
Status : Active
Type : II
Certificate Number : R0-CEP 2020-194 - Rev 00
Issue Date : 2022-06-23
Type : Chemical
Substance Number : 353
Status : Valid
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm :
NDC Package Code : 22552-0025
Start Marketing Date : 2011-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-28
Pay. Date : 2013-01-03
DMF Number : 3535
Submission : 1979-06-04
Status : Active
Type : II
Certificate Number : R0-CEP 2022-147 - Rev 00
Issue Date : 2022-09-02
Type : Chemical
Substance Number : 353
Status : Valid
Registration Number : 218MF10379
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration :
NDC Package Code : 82298-104
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Handok Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-71-B-197-03
Manufacturer Name : EUROAPI France
Manufacturer Address : 63480 Vertolyae, France
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40755
Submission : 2024-10-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8855
Submission : 1990-11-26
Status : Active
Type : II
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 : 2021-05-06
Pay. Date : 2021-04-09
DMF Number : 34505
Submission : 2020-02-21
Status : Active
Type : II
Date of Issue : 2022-07-05
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm :
NDC Package Code : 22552-0025
Start Marketing Date : 2011-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
13
PharmaCompass offers a list of Prednisolone 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 Prednisolone manufacturer or Prednisolone supplier for your needs.
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A Prednisolone Tebutate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prednisolone Tebutate, including repackagers and relabelers. The FDA regulates Prednisolone Tebutate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prednisolone Tebutate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Prednisolone Tebutate supplier is an individual or a company that provides Prednisolone Tebutate active pharmaceutical ingredient (API) or Prednisolone Tebutate finished formulations upon request. The Prednisolone Tebutate suppliers may include Prednisolone Tebutate API manufacturers, exporters, distributors and traders.
click here to find a list of Prednisolone Tebutate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 36 companies offering Prednisolone Tebutate
Get in contact with the supplier of your choice: