01 3BASF
02 1F. Hoffmann-La Roche
03 1Blank
01 1BETA CAROTENE
02 1BETA-CAROTENE (25MG.) SOFT GELATIN CAPSULES
03 1BETA-CAROTENE CAPS., 30MG AS PRODUCED IN NUTLEY,NJ FACILITIES
04 1BETA-CAROTENE CAPSULES,50MG.
05 1LUROTIN TM BETA-CAROTENE (DRY POWDER FORMULATION)
01 3Germany
02 1Switzerland
03 1Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5865
Submission : 1985-05-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5851
Submission : 1985-05-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5793
Submission : 1985-04-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4390
Submission : 1982-01-14
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7653
Submission : 1988-08-24
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
69
PharmaCompass offers a list of Beta Carotene 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 Beta Carotene manufacturer or Beta Carotene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Beta Carotene manufacturer or Beta Carotene supplier.
PharmaCompass also assists you with knowing the Beta Carotene API Price utilized in the formulation of products. Beta Carotene API Price is not always fixed or binding as the Beta Carotene Price is obtained through a variety of data sources. The Beta Carotene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E160A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E160A, including repackagers and relabelers. The FDA regulates E160A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E160A 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 E160A manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E160A supplier is an individual or a company that provides E160A active pharmaceutical ingredient (API) or E160A finished formulations upon request. The E160A suppliers may include E160A API manufacturers, exporters, distributors and traders.
click here to find a list of E160A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E160A DMF (Drug Master File) is a document detailing the whole manufacturing process of E160A active pharmaceutical ingredient (API) in detail. Different forms of E160A DMFs exist exist since differing nations have different regulations, such as E160A USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A E160A DMF submitted to regulatory agencies in the US is known as a USDMF. E160A USDMF includes data on E160A's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The E160A USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of E160A suppliers with USDMF on PharmaCompass.
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