Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
01 2Bayer AG
02 1Alivus Life Sciences
03 2BASF
04 1Flamma SpA
05 1Taro Pharmaceutical Industries
06 1Zhejiang Huahai Pharmaceutical
01 4AZELAIC ACID
02 1AZELAIC ACID (A)
03 1AZELAIC ACID, MICRONIZED
04 1DERMAZ 88 (AZELAIC ACID)
05 1DERMAZ 99 (AZELAIC ACID)
01 1China
02 4Germany
03 1India
04 1Italy
05 1U.S.A
01 8Active
01 4Complete
02 4Blank
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9289
Submission : 1991-08-07
Status : Active
Type : II
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28190
Submission : 2014-06-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-15
Pay. Date : 2016-03-10
DMF Number : 29924
Submission : 2016-03-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-11-24
Pay. Date : 2014-11-11
DMF Number : 19481
Submission : 2006-05-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11615
Submission : 1995-08-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38042
Submission : 2023-02-24
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-02-05
Pay. Date : 2015-11-30
DMF Number : 29484
Submission : 2015-12-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-01-17
Pay. Date : 2019-09-30
DMF Number : 33485
Submission : 2019-09-17
Status : Active
Type : II
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A NCGC00014993-06 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00014993-06, including repackagers and relabelers. The FDA regulates NCGC00014993-06 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00014993-06 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 NCGC00014993-06 supplier is an individual or a company that provides NCGC00014993-06 active pharmaceutical ingredient (API) or NCGC00014993-06 finished formulations upon request. The NCGC00014993-06 suppliers may include NCGC00014993-06 API manufacturers, exporters, distributors and traders.
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A NCGC00014993-06 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00014993-06 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00014993-06 DMFs exist exist since differing nations have different regulations, such as NCGC00014993-06 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NCGC00014993-06 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00014993-06 USDMF includes data on NCGC00014993-06's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00014993-06 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 6 companies offering NCGC00014993-06
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