01 1BASF
02 1MLA Group of Industries
03 1Pfizer Inc
01 1ETHYLENE GLYCOL STEARATE (EGMS/EGDS) USP
02 1PLEXIGEL (POLYETHYLENE OINT. BASE)
03 1POLYETHYLENE GLYCOL 3350
01 1Germany
02 1India
03 1U.S.A
01 2Active
02 1Inactive
01 1Complete
02 2Blank
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-10
Pay. Date : 2013-08-29
DMF Number : 16946
Submission : 2003-11-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38354
Submission : 2023-05-08
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2358
Submission : 1974-11-18
Status : Inactive
Type : II
39
PharmaCompass offers a list of Polyethylene Glycol Monostearate 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 Polyethylene Glycol Monostearate manufacturer or Polyethylene Glycol Monostearate supplier for your needs.
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PharmaCompass also assists you with knowing the Polyethylene Glycol Monostearate API Price utilized in the formulation of products. Polyethylene Glycol Monostearate API Price is not always fixed or binding as the Polyethylene Glycol Monostearate Price is obtained through a variety of data sources. The Polyethylene Glycol Monostearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A cremophor S9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cremophor S9, including repackagers and relabelers. The FDA regulates cremophor S9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cremophor S9 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 cremophor S9 supplier is an individual or a company that provides cremophor S9 active pharmaceutical ingredient (API) or cremophor S9 finished formulations upon request. The cremophor S9 suppliers may include cremophor S9 API manufacturers, exporters, distributors and traders.
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A cremophor S9 DMF (Drug Master File) is a document detailing the whole manufacturing process of cremophor S9 active pharmaceutical ingredient (API) in detail. Different forms of cremophor S9 DMFs exist exist since differing nations have different regulations, such as cremophor S9 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A cremophor S9 DMF submitted to regulatory agencies in the US is known as a USDMF. cremophor S9 USDMF includes data on cremophor S9's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The cremophor S9 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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