Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 1Synnat Pharma
02 1Temad Co
03 1LGM Pharma
04 1DKSH
05 1Jai Radhe Sales
06 1Faran Shimi Pharmaceutical
07 1Parand Darou Pharma
08 1Alkaloids Corporation
09 1Biotechnica DWC
10 1Guangzhou Tosun Pharmaceutical
11 2Inga Pharmaceuticals
12 1Kimyagaran
13 2Recordati
14 1Saurav Chemicals
15 1Sichuan Renan Pharmaceutical
16 1elm-plastic GmbH
17 4Blank
01 1Algeria
02 2China
03 1Germany
04 6India
05 4Iran
06 2Italy
07 1Switzerland
08 1U.S.A
09 4Blank
01 1Active
02 6Inactive
03 15Blank
01 22Blank
01 1231MF10018
02 21Blank
01 1WC-0171A3
02 1WC-301n
03 20Blank
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Date of Issue : 2021-06-03
Valid Till : 2024-02-07
Written Confirmation Number : WC-301n
Address of the Firm :
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3633
Submission : 1979-10-15
Status : Active
Type : II
NDC Package Code : 12711-7480
Start Marketing Date : 2001-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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 : 3309
Submission : 1978-06-15
Status : Inactive
Type : II
Registration Number : 231MF10018
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2019-01-29
Latest Date of Registration : --
NDC Package Code : 12711-7480
Start Marketing Date : 2001-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 63570-030
Start Marketing Date : 2023-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63570-030
Start Marketing Date : 2023-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Date of Issue : 2021-08-27
Valid Till : 2022-08-13
Written Confirmation Number : WC-0171A3
Address of the Firm :
NDC Package Code : 43235-0009
Start Marketing Date : 2018-09-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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.
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