01 1Bayer AG
02 1Cerestar USA Inc
03 1Pharmatech
04 1Roquette
05 2Wacker Chemie AG
01 12-HYDROXYPROPYL-B-CYCLODEXTRIN
02 1BETA CYCLODEXTRIN
03 2BETA-CYCLODEXTRIN
04 1METHYL BETA-CYCLODEXTRIN
05 1NOCLOPROST BETA-CYCLODEXTRIN CLATHRATE
01 1France
02 3Germany
03 1U.S.A
04 1United Kingdom
01 3Active
02 3Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8423
Submission : 1990-02-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9403
Submission : 1991-10-21
Status : Inactive
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7435
Submission : 1988-04-14
Status : Inactive
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9155
Submission : 1991-06-10
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15489
Submission : 2001-06-15
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14620
Submission : 1999-12-08
Status : Active
Type : IV
68
PharmaCompass offers a list of Beta-Cyclodextrin API 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 Beta-Cyclodextrin API manufacturer or Beta-Cyclodextrin API supplier for your needs.
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A EC 231-493-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EC 231-493-2, including repackagers and relabelers. The FDA regulates EC 231-493-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EC 231-493-2 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A EC 231-493-2 supplier is an individual or a company that provides EC 231-493-2 active pharmaceutical ingredient (API) or EC 231-493-2 finished formulations upon request. The EC 231-493-2 suppliers may include EC 231-493-2 API manufacturers, exporters, distributors and traders.
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A EC 231-493-2 DMF (Drug Master File) is a document detailing the whole manufacturing process of EC 231-493-2 active pharmaceutical ingredient (API) in detail. Different forms of EC 231-493-2 DMFs exist exist since differing nations have different regulations, such as EC 231-493-2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EC 231-493-2 DMF submitted to regulatory agencies in the US is known as a USDMF. EC 231-493-2 USDMF includes data on EC 231-493-2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EC 231-493-2 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EC 231-493-2 suppliers with USDMF on PharmaCompass.
We have 5 companies offering EC 231-493-2
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