Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1Nuray Chemicals Private Limited
02 1Cohance Lifesciences
03 1Atul Limited
04 1Chongqing Huapont Pharmaceutical
05 1Dipharma
06 1Extrovis AG
07 1H. Lundbeck AS
08 1Jacobus Pharmaceutical Company, Inc
09 2Macleods Pharmaceuticals Limited
10 2Medilux Laboratories
11 1Regis Technologies
12 1Sai Life Sciences Limited
13 1Taro Pharmaceutical Industries
01 5DAPSONE
02 1DAPSONE (FINAL DOSAGE FORMS)
03 8DAPSONE USP
04 1DAPSONE, USP
01 1China
02 1Denmark
03 8India
04 1Italy
05 1Switzerland
06 3U.S.A
01 12Active
02 3Inactive
01 6Complete
02 9Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-16
Pay. Date : 2013-12-13
DMF Number : 27678
Submission : 2013-12-13
Status : Active
Type : II
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35342
Submission : 2020-10-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-08-12
Pay. Date : 2013-02-26
DMF Number : 17781
Submission : 2004-10-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-02-04
Pay. Date : 2019-10-30
DMF Number : 31521
Submission : 2017-06-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33630
Submission : 2019-03-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15065
Submission : 2000-09-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2022-03-29
Pay. Date : 2022-03-21
DMF Number : 35244
Submission : 2021-12-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33228
Submission : 2019-01-16
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-07-30
Pay. Date : 2014-01-16
DMF Number : 27701
Submission : 2013-11-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-20
Pay. Date : 2016-03-29
DMF Number : 29999
Submission : 2016-03-31
Status : Active
Type : II
A Dapsone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dapsone, including repackagers and relabelers. The FDA regulates Dapsone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dapsone 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 Dapsone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dapsone supplier is an individual or a company that provides Dapsone active pharmaceutical ingredient (API) or Dapsone finished formulations upon request. The Dapsone suppliers may include Dapsone API manufacturers, exporters, distributors and traders.
click here to find a list of Dapsone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dapsone DMF (Drug Master File) is a document detailing the whole manufacturing process of Dapsone active pharmaceutical ingredient (API) in detail. Different forms of Dapsone DMFs exist exist since differing nations have different regulations, such as Dapsone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dapsone DMF submitted to regulatory agencies in the US is known as a USDMF. Dapsone USDMF includes data on Dapsone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dapsone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dapsone suppliers with USDMF on PharmaCompass.
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