Veranova: A CDMO that manages complexity with confidence.
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01 1Veranova
02 1Aspen API
03 1American Pacific Corporation
04 1Apothecon Pharmaceuticals
05 1Cilag AG
06 1Yichang Humanwell Pharmaceutical
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01 1REMIFENTANIL HCL
02 1REMIFENTANIL HCL DRUG SUBSTANCE
03 4REMIFENTANIL HYDROCHLORIDE
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01 1China
02 1India
03 1Netherlands
04 1Switzerland
05 2U.S.A
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01 6Active
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01 5Complete
02 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25811
Submission : 2011-12-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-03-30
Pay. Date : 2014-12-04
DMF Number : 28106
Submission : 2014-03-13
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-04-14
Pay. Date : 2021-02-17
DMF Number : 34303
Submission : 2020-11-18
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-04-07
Pay. Date : 2016-09-26
DMF Number : 30156
Submission : 2016-09-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-28
Pay. Date : 2013-09-26
DMF Number : 27513
Submission : 2013-09-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-08-21
Pay. Date : 2018-09-28
DMF Number : 33151
Submission : 2018-09-21
Status : Active
Type : II
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PharmaCompass offers a list of Remifentanil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Remifentanil manufacturer or Remifentanil supplier for your needs.
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A 132875-61-7 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 132875-61-7 (Parent), including repackagers and relabelers. The FDA regulates 132875-61-7 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 132875-61-7 (Parent) 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 132875-61-7 (Parent) supplier is an individual or a company that provides 132875-61-7 (Parent) active pharmaceutical ingredient (API) or 132875-61-7 (Parent) finished formulations upon request. The 132875-61-7 (Parent) suppliers may include 132875-61-7 (Parent) API manufacturers, exporters, distributors and traders.
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A 132875-61-7 (Parent) DMF (Drug Master File) is a document detailing the whole manufacturing process of 132875-61-7 (Parent) active pharmaceutical ingredient (API) in detail. Different forms of 132875-61-7 (Parent) DMFs exist exist since differing nations have different regulations, such as 132875-61-7 (Parent) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 132875-61-7 (Parent) DMF submitted to regulatory agencies in the US is known as a USDMF. 132875-61-7 (Parent) USDMF includes data on 132875-61-7 (Parent)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 132875-61-7 (Parent) USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 6 companies offering 132875-61-7 (Parent)
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