01 13M Company
02 13M Drug Delivery Systems
03 1ACS DOBFAR SPA
04 1Laboratorio Syntex S.A
05 1SIMS Srl
01 1CORDRAN (FLURANDRENOLIDE) TAPE
02 1FLURANDRENOLIDE
03 1FLURANDRENOLIDE DRUG-IN-ADHESIVE R-2813
04 1FLURANDRENOLIDE USP BULK FORM (NON-STERILE)
05 1FLURANDRENOLONE
01 1Argentina
02 2Italy
03 2U.S.A
01 2Active
02 3Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38706
Submission : 2024-01-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2757
Submission : 1976-10-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5063
Submission : 1983-09-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 414
Submission : 1960-12-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4107
Submission : 1981-03-03
Status : Inactive
Type : II
13
PharmaCompass offers a list of Flurandrenolone 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 Flurandrenolone manufacturer or Flurandrenolone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flurandrenolone manufacturer or Flurandrenolone supplier.
PharmaCompass also assists you with knowing the Flurandrenolone API Price utilized in the formulation of products. Flurandrenolone API Price is not always fixed or binding as the Flurandrenolone Price is obtained through a variety of data sources. The Flurandrenolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Drenison manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Drenison, including repackagers and relabelers. The FDA regulates Drenison manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Drenison 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 Drenison manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Drenison supplier is an individual or a company that provides Drenison active pharmaceutical ingredient (API) or Drenison finished formulations upon request. The Drenison suppliers may include Drenison API manufacturers, exporters, distributors and traders.
click here to find a list of Drenison suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Drenison DMF (Drug Master File) is a document detailing the whole manufacturing process of Drenison active pharmaceutical ingredient (API) in detail. Different forms of Drenison DMFs exist exist since differing nations have different regulations, such as Drenison USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Drenison DMF submitted to regulatory agencies in the US is known as a USDMF. Drenison USDMF includes data on Drenison's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Drenison USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Drenison suppliers with USDMF on PharmaCompass.
We have 5 companies offering Drenison
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