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 1Aurobindo Pharma Limited
04 1CSPC New Nova Pharmaceutical
05 1Hikal
06 1Ipca Laboratories
07 1Labochem Ltd
08 1POLI INDUSTRIA CHIMICA SPA
09 2Perrigo API India Private Limited
10 1Plantex Ltd.
11 1Sun Pharmaceutical Industries Limited
12 1Zentiva
13 1Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Complete
Rev. Date : 2014-12-16
Pay. Date : 2014-11-28
DMF Number : 20976
Submission : 2007-10-26
Status :
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 : 12562
Submission : 1997-06-26
Status :
Type : II
A Pentoxifylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentoxifylline, including repackagers and relabelers. The FDA regulates Pentoxifylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentoxifylline 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 Pentoxifylline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pentoxifylline supplier is an individual or a company that provides Pentoxifylline active pharmaceutical ingredient (API) or Pentoxifylline finished formulations upon request. The Pentoxifylline suppliers may include Pentoxifylline API manufacturers, exporters, distributors and traders.
click here to find a list of Pentoxifylline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pentoxifylline DMF (Drug Master File) is a document detailing the whole manufacturing process of Pentoxifylline active pharmaceutical ingredient (API) in detail. Different forms of Pentoxifylline DMFs exist exist since differing nations have different regulations, such as Pentoxifylline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pentoxifylline DMF submitted to regulatory agencies in the US is known as a USDMF. Pentoxifylline USDMF includes data on Pentoxifylline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pentoxifylline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pentoxifylline suppliers with USDMF on PharmaCompass.
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