Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1Symbiotec Pharmalab
02 1Gonane Pharma
03 1Sanofi
04 1Transo-Pharm Handels GmbH
05 1Aspen API
06 1Swati Spentose
07 1AASraw Biochemical Technology Co., Ltd
08 1ASG Biochem
09 1Androst Biotech
10 1Balaji Corporation
11 3Bayer AG
12 1Cohesion Biotec
13 2Fareva
14 1Fujifilm Diosynth Biotechnologies
15 1Gedeon Richter
16 1Hangzhou Deli Chemical
17 1Ipca Laboratories
18 1Lupin Ltd
19 1Pcca
20 2Shakti Lifescience
21 1Steroid SpA
22 1Zhejiang Xianju Pharmaceutical Co. Ltd
23 3Blank
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01 3China
02 1France
03 4Germany
04 1Hungary
05 11India
06 1Italy
07 2Luxembourg
08 1Netherlands
09 2United Kingdom
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01 4Active
02 3Inactive
03 22Blank
01 4Valid
02 25Blank
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01 1303MF10163
02 28Blank
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01 1WC-0402A2
02 28Blank
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01 120121228-181-I-165-04
02 120121228-181-I-165-04(1)
03 120121228-181-I-165-04(2)
04 120220526-181-I-638-07
05 25Blank
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01 112866-1008
02 124823-905
03 124823-906
04 143647-145
05 149803-013
06 151508-019
07 151927-0076
08 160722-3022
09 160870-0276
10 173377-063
11 173774-004
12 173774-011
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01 13567
02 28Blank
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3072
Submission : 1977-11-09
Status : Inactive
Type : II
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-06
Pay. Date : 2014-12-22
DMF Number : 12268
Submission : 1996-12-16
Status : Active
Type : II
Certificate Number : CEP 2009-171 - Rev 02
Issue Date : 2025-04-25
Type : Chemical
Substance Number : 1614
Status : Valid
NDC Package Code : 60870-0276
Start Marketing Date : 1980-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Synex Co., Ltd.
Registration Date : 2022-05-26
Registration Number : 20220526-181-I-638-07
Manufacturer Name : Aspen Oss BV@Aspen Oss BV
Manufacturer Address : Kloosterstraat 6, Oss, 5349 AB, The Netherlands@Veersemeer 4, Oss, 5347 JN, The Netherlands
Available Reg Filing : ASMF, BR |
SWATI – Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39594
Submission : 2024-03-20
Status : Active
Type : II
NDC Package Code : 49803-013
Start Marketing Date : 2024-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25000g/25000g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-06-02
Pay. Date : 2017-04-04
DMF Number : 23948
Submission : 2010-07-02
Status : Active
Type : II
Registration Number : 303MF10163
Registrant's Address : Parc Industriel d'Incarville Parc de la Fringale CS 10606 27106 Val de Reuil Cedex France
Initial Date of Registration : 2021-11-10
Latest Date of Registration :
NDC Package Code : 24823-906
Start Marketing Date : 2011-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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 : 4267
Submission : 1981-09-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24553
Submission : 2011-01-18
Status : Inactive
Type : II
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PharmaCompass offers a list of Estradiol Valerate 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 Estradiol Valerate manufacturer or Estradiol Valerate supplier for your needs.
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A Neofollin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neofollin, including repackagers and relabelers. The FDA regulates Neofollin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neofollin 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 Neofollin supplier is an individual or a company that provides Neofollin active pharmaceutical ingredient (API) or Neofollin finished formulations upon request. The Neofollin suppliers may include Neofollin API manufacturers, exporters, distributors and traders.
click here to find a list of Neofollin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 22 companies offering Neofollin
Get in contact with the supplier of your choice: