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01 1Alivus Life Sciences
02 1Aurobindo Pharma Limited
03 1Dasami Lab
04 1Zydus Lifesciences
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01 4GABAPENTIN ENACARBIL
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01 4India
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01 4Active
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01 3Complete
02 1Blank
GDUFA
DMF Review : Complete
Rev. Date : 2018-11-21
Pay. Date : 2018-11-02
DMF Number : 33296
Submission : 2018-11-02
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2023-12-20
Pay. Date : 2023-11-29
DMF Number : 39197
Submission : 2023-12-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-05-10
Pay. Date : 2019-02-21
DMF Number : 33386
Submission : 2019-03-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41053
Submission : 2024-12-30
Status : Active
Type : II
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PharmaCompass offers a list of Gabapentin Enacarbil 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 Gabapentin Enacarbil manufacturer or Gabapentin Enacarbil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gabapentin Enacarbil manufacturer or Gabapentin Enacarbil supplier.
PharmaCompass also assists you with knowing the Gabapentin Enacarbil API Price utilized in the formulation of products. Gabapentin Enacarbil API Price is not always fixed or binding as the Gabapentin Enacarbil Price is obtained through a variety of data sources. The Gabapentin Enacarbil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Q-1947 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Q-1947, including repackagers and relabelers. The FDA regulates Q-1947 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Q-1947 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 Q-1947 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Q-1947 supplier is an individual or a company that provides Q-1947 active pharmaceutical ingredient (API) or Q-1947 finished formulations upon request. The Q-1947 suppliers may include Q-1947 API manufacturers, exporters, distributors and traders.
click here to find a list of Q-1947 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Q-1947 DMF (Drug Master File) is a document detailing the whole manufacturing process of Q-1947 active pharmaceutical ingredient (API) in detail. Different forms of Q-1947 DMFs exist exist since differing nations have different regulations, such as Q-1947 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Q-1947 DMF submitted to regulatory agencies in the US is known as a USDMF. Q-1947 USDMF includes data on Q-1947's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Q-1947 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Q-1947 suppliers with USDMF on PharmaCompass.
We have 4 companies offering Q-1947
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