Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
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01 1Apex Healthcare Limited
02 1Cambrex Corporation
03 1Dishman Carbogen Amcis
04 1Erregierre SpA
05 1Kreative Organics
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01 2BISACODYL
02 2BISACODYL USP
03 1BISACODYL USP-EP
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01 3India
02 1Italy
03 1U.S.A
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01 5Active
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01 5Blank
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 : 36474
Submission : 2022-01-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2248
Submission : 1974-03-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20476
Submission : 2007-04-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14947
Submission : 2000-06-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16058
Submission : 2002-06-28
Status : Active
Type : II
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A Neolax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neolax, including repackagers and relabelers. The FDA regulates Neolax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neolax 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 Neolax supplier is an individual or a company that provides Neolax active pharmaceutical ingredient (API) or Neolax finished formulations upon request. The Neolax suppliers may include Neolax API manufacturers, exporters, distributors and traders.
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A Neolax DMF (Drug Master File) is a document detailing the whole manufacturing process of Neolax active pharmaceutical ingredient (API) in detail. Different forms of Neolax DMFs exist exist since differing nations have different regulations, such as Neolax USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Neolax DMF submitted to regulatory agencies in the US is known as a USDMF. Neolax USDMF includes data on Neolax's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Neolax USDMF is kept confidential to protect the manufacturer’s intellectual property.
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