DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 1TAPI Technology & API Services
03 1Cadila Pharmaceuticals
04 2Cipla
05 1Divis Laboratories
06 1Glenmark Life Sciences
07 1Hainan Poly Pharm
08 1Lupin Ltd
09 1Morepen Laboratories
10 1Orchid Pharma
11 1RANBAXY LABORATORIES LIMITED
12 1Sun Pharmaceutical Industries Limited
13 1Taro Pharmaceutical Industries
14 1Vasudha Pharma Chem
15 1Viatris
01 9DESLORATADINE
02 2DESLORATADINE DRUG SUBSTANCE
03 1DESLORATADINE FORM I: FORM II (89:11)
04 4DESLORATADINE USP
01 1China
02 12India
03 1Israel
04 2U.S.A
01 10Active
02 6Inactive
01 3Complete
02 13Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19456
Submission : 2006-05-24
Status : Active
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19403
Submission : 2006-05-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21133
Submission : 2007-12-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19428
Submission : 2006-05-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19083
Submission : 2005-12-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-16
Pay. Date : 2014-01-10
DMF Number : 17652
Submission : 2004-09-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19339
Submission : 2006-04-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19014
Submission : 2005-12-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24275
Submission : 2010-12-14
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-10-14
Pay. Date : 2015-09-28
DMF Number : 21187
Submission : 2007-12-21
Status : Active
Type : II
A Desloratadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desloratadine, including repackagers and relabelers. The FDA regulates Desloratadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desloratadine 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 Desloratadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desloratadine supplier is an individual or a company that provides Desloratadine active pharmaceutical ingredient (API) or Desloratadine finished formulations upon request. The Desloratadine suppliers may include Desloratadine API manufacturers, exporters, distributors and traders.
click here to find a list of Desloratadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Desloratadine DMF (Drug Master File) is a document detailing the whole manufacturing process of Desloratadine active pharmaceutical ingredient (API) in detail. Different forms of Desloratadine DMFs exist exist since differing nations have different regulations, such as Desloratadine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Desloratadine DMF submitted to regulatory agencies in the US is known as a USDMF. Desloratadine USDMF includes data on Desloratadine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Desloratadine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Desloratadine suppliers with USDMF on PharmaCompass.
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