01 4St. Gobain Performance Plastics
01 1TYGON (R)R 3350 - SANITARY SILICONE TUBING
02 1TYGON S-50-HL MEDICAL/SURGICAL TUBING
03 1TYGON(R) S-50-HL MEDICAL/SURGICAL TUBING
04 1TYGONr 2475 HIGH PURITY TUBING AND TYGONr 2475 I.B. HIGH PURITY PRESSURE TUBING
01 4France
01 4Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19844
Submission : 2006-10-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19475
Submission : 2006-05-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25831
Submission : 2012-02-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20743
Submission : 2007-07-25
Status : Inactive
Type : II
47
PharmaCompass offers a list of Pevikon 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 Pevikon manufacturer or Pevikon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pevikon manufacturer or Pevikon supplier.
PharmaCompass also assists you with knowing the Pevikon API Price utilized in the formulation of products. Pevikon API Price is not always fixed or binding as the Pevikon Price is obtained through a variety of data sources. The Pevikon Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rhodopas 6000 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rhodopas 6000, including repackagers and relabelers. The FDA regulates Rhodopas 6000 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rhodopas 6000 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Rhodopas 6000 supplier is an individual or a company that provides Rhodopas 6000 active pharmaceutical ingredient (API) or Rhodopas 6000 finished formulations upon request. The Rhodopas 6000 suppliers may include Rhodopas 6000 API manufacturers, exporters, distributors and traders.
click here to find a list of Rhodopas 6000 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rhodopas 6000 DMF (Drug Master File) is a document detailing the whole manufacturing process of Rhodopas 6000 active pharmaceutical ingredient (API) in detail. Different forms of Rhodopas 6000 DMFs exist exist since differing nations have different regulations, such as Rhodopas 6000 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rhodopas 6000 DMF submitted to regulatory agencies in the US is known as a USDMF. Rhodopas 6000 USDMF includes data on Rhodopas 6000's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rhodopas 6000 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rhodopas 6000 suppliers with USDMF on PharmaCompass.
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