01 2Recordati
02 1elm-plastic GmbH
03 4Blank
01 1PAPAVERINE BASE
02 1PAPAVERINE HCI
03 1PAPAVERINE HCL-METHODS, FACIL,CONTRL-IN MFGR OF T.R. CAPS
04 1PAPAVERINE HCL-TIME RELEASE PELLETS (BULK)
05 1PAPAVERINE HYDROCHLORIDE
06 1PAVABID (R) HP CAPULETS,300MG
07 1PAVABID-PB TIMED RELEASE CAPSULES
01 1Germany
02 2Italy
03 4Blank
01 1Active
02 6Inactive
01 7Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2426
Submission : 1975-03-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3633
Submission : 1979-10-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3309
Submission : 1978-06-15
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1006
Submission : 1966-11-04
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 830
Submission : 1964-08-27
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 822
Submission : 1964-07-02
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3863
Submission : 1980-07-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Papaverine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Papaverine, including repackagers and relabelers. The FDA regulates Papaverine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Papaverine 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 Papaverine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Papaverine supplier is an individual or a company that provides Papaverine active pharmaceutical ingredient (API) or Papaverine finished formulations upon request. The Papaverine suppliers may include Papaverine API manufacturers, exporters, distributors and traders.
click here to find a list of Papaverine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Papaverine DMF (Drug Master File) is a document detailing the whole manufacturing process of Papaverine active pharmaceutical ingredient (API) in detail. Different forms of Papaverine DMFs exist exist since differing nations have different regulations, such as Papaverine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Papaverine DMF submitted to regulatory agencies in the US is known as a USDMF. Papaverine USDMF includes data on Papaverine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Papaverine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Papaverine suppliers with USDMF on PharmaCompass.
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