Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
01 1Apex Healthcare Limited
02 1Arch Pharmalabs
03 1Dipharma
04 1Esteve Quimica
05 1F.I.S. Fabbrica Italiana Sintetici
06 1Krka
07 1Ramdev Chemicals Pvt Ltd
08 1Sifavitor srl
09 1Unichem Laboratories Limited
10 1Wockhardt
11 3Blank
Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36841
Submission : 2022-02-25
Status :
Type : II
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A Feldene Gel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Feldene Gel, including repackagers and relabelers. The FDA regulates Feldene Gel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Feldene Gel 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 Feldene Gel supplier is an individual or a company that provides Feldene Gel active pharmaceutical ingredient (API) or Feldene Gel finished formulations upon request. The Feldene Gel suppliers may include Feldene Gel API manufacturers, exporters, distributors and traders.
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A Feldene Gel DMF (Drug Master File) is a document detailing the whole manufacturing process of Feldene Gel active pharmaceutical ingredient (API) in detail. Different forms of Feldene Gel DMFs exist exist since differing nations have different regulations, such as Feldene Gel USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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