Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1TAPI Technology & API Services
03 1Apotex Pharmachem
04 1Lupin Ltd
05 1Macleods Pharmaceuticals Limited
06 1Viatris
07 2Wanbury Limited
08 1Zhejiang Huahai Pharmaceutical
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Complete
Rev. Date : 2017-01-19
Pay. Date : 2016-12-07
DMF Number : 20633
Submission : 2007-06-26
Status :
Type : II
TAPI offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-06
Pay. Date : 2012-11-13
DMF Number : 23312
Submission : 2009-11-25
Status :
Type : II
A Carvedilol Phosphate Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carvedilol Phosphate Hemihydrate, including repackagers and relabelers. The FDA regulates Carvedilol Phosphate Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carvedilol Phosphate Hemihydrate 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 Carvedilol Phosphate Hemihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carvedilol Phosphate Hemihydrate supplier is an individual or a company that provides Carvedilol Phosphate Hemihydrate active pharmaceutical ingredient (API) or Carvedilol Phosphate Hemihydrate finished formulations upon request. The Carvedilol Phosphate Hemihydrate suppliers may include Carvedilol Phosphate Hemihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Carvedilol Phosphate Hemihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carvedilol Phosphate Hemihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Carvedilol Phosphate Hemihydrate active pharmaceutical ingredient (API) in detail. Different forms of Carvedilol Phosphate Hemihydrate DMFs exist exist since differing nations have different regulations, such as Carvedilol Phosphate Hemihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carvedilol Phosphate Hemihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Carvedilol Phosphate Hemihydrate USDMF includes data on Carvedilol Phosphate Hemihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carvedilol Phosphate Hemihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carvedilol Phosphate Hemihydrate suppliers with USDMF on PharmaCompass.
We have 8 companies offering Carvedilol Phosphate Hemihydrate
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