01 1Celanese
02 1Innovative Pharmacy Solutions
03 1Katwijk Chemie
04 1Mallinckrodt Pharmaceuticals
05 1ORGAMOL PHARMA SOLUTIONS SA
06 1Pliva Hrvatska
01 4PEMOLINE
02 1PEMOLINE 18.75 MG COMPOUNDED CAPSULES
03 1PEMOLINE MALLINCKRODT CODE 1500
01 1Croatia
02 1Ireland
03 1Netherlands
04 1Switzerland
05 2U.S.A
01 1Active
02 5Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12238
Submission : 1996-12-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31268
Submission : 2016-12-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11780
Submission : 1995-12-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13865
Submission : 1998-11-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12796
Submission : 1997-12-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13919
Submission : 1998-12-29
Status : Inactive
Type : II
85
PharmaCompass offers a list of Pemoline 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 Pemoline manufacturer or Pemoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pemoline manufacturer or Pemoline supplier.
PharmaCompass also assists you with knowing the Pemoline API Price utilized in the formulation of products. Pemoline API Price is not always fixed or binding as the Pemoline Price is obtained through a variety of data sources. The Pemoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hyton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyton, including repackagers and relabelers. The FDA regulates Hyton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyton 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 Hyton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hyton supplier is an individual or a company that provides Hyton active pharmaceutical ingredient (API) or Hyton finished formulations upon request. The Hyton suppliers may include Hyton API manufacturers, exporters, distributors and traders.
click here to find a list of Hyton suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hyton DMF (Drug Master File) is a document detailing the whole manufacturing process of Hyton active pharmaceutical ingredient (API) in detail. Different forms of Hyton DMFs exist exist since differing nations have different regulations, such as Hyton USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hyton DMF submitted to regulatory agencies in the US is known as a USDMF. Hyton USDMF includes data on Hyton's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hyton USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hyton suppliers with USDMF on PharmaCompass.
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