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01 1BASF
02 1Royal DSM
03 1Zhejiang NHU Co
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01 1VITAMIN A PALMITATE
02 1VITAMIN A PALMITATE 1.7 MIU/G (WITHOUT STABILIZERS)
03 1VITAMIN A PALMITATE/VITAMIN E OIL/SOYBEAN SALAD OIL BLEND
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01 1China
02 1Germany
03 1Netherlands
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01 2Active
02 1Inactive
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01 1Complete
02 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6581
Submission : 1986-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-07-14
Pay. Date : 2017-01-10
DMF Number : 31038
Submission : 2016-10-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17708
Submission : 2004-09-14
Status : Active
Type : II
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PharmaCompass offers a list of Vitamin A Palmitate 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 Vitamin A Palmitate manufacturer or Vitamin A Palmitate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A Palmitate manufacturer or Vitamin A Palmitate supplier.
PharmaCompass also assists you with knowing the Vitamin A Palmitate API Price utilized in the formulation of products. Vitamin A Palmitate API Price is not always fixed or binding as the Vitamin A Palmitate Price is obtained through a variety of data sources. The Vitamin A Palmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALL-(E)-RETINOL PALMITATE [WHO-IP] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALL-(E)-RETINOL PALMITATE [WHO-IP], including repackagers and relabelers. The FDA regulates ALL-(E)-RETINOL PALMITATE [WHO-IP] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALL-(E)-RETINOL PALMITATE [WHO-IP] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of ALL-(E)-RETINOL PALMITATE [WHO-IP] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALL-(E)-RETINOL PALMITATE [WHO-IP] supplier is an individual or a company that provides ALL-(E)-RETINOL PALMITATE [WHO-IP] active pharmaceutical ingredient (API) or ALL-(E)-RETINOL PALMITATE [WHO-IP] finished formulations upon request. The ALL-(E)-RETINOL PALMITATE [WHO-IP] suppliers may include ALL-(E)-RETINOL PALMITATE [WHO-IP] API manufacturers, exporters, distributors and traders.
click here to find a list of ALL-(E)-RETINOL PALMITATE [WHO-IP] suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ALL-(E)-RETINOL PALMITATE [WHO-IP] DMF (Drug Master File) is a document detailing the whole manufacturing process of ALL-(E)-RETINOL PALMITATE [WHO-IP] active pharmaceutical ingredient (API) in detail. Different forms of ALL-(E)-RETINOL PALMITATE [WHO-IP] DMFs exist exist since differing nations have different regulations, such as ALL-(E)-RETINOL PALMITATE [WHO-IP] USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ALL-(E)-RETINOL PALMITATE [WHO-IP] DMF submitted to regulatory agencies in the US is known as a USDMF. ALL-(E)-RETINOL PALMITATE [WHO-IP] USDMF includes data on ALL-(E)-RETINOL PALMITATE [WHO-IP]'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ALL-(E)-RETINOL PALMITATE [WHO-IP] USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ALL-(E)-RETINOL PALMITATE [WHO-IP] suppliers with USDMF on PharmaCompass.
We have 3 companies offering ALL-(E)-RETINOL PALMITATE [WHO-IP]
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