Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
01 1Apex Healthcare Limited
02 1Cambrex Corporation
03 1Dishman Carbogen Amcis
04 1Erregierre SpA
05 1Kreative Organics
01 2BISACODYL
02 2BISACODYL USP
03 1BISACODYL USP-EP
01 3India
02 1Italy
03 1U.S.A
01 5Active
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 LS-2218 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-2218, including repackagers and relabelers. The FDA regulates LS-2218 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-2218 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 LS-2218 DMF (Drug Master File) is a document detailing the whole manufacturing process of LS-2218 active pharmaceutical ingredient (API) in detail. Different forms of LS-2218 DMFs exist exist since differing nations have different regulations, such as LS-2218 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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