Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
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01 1Synnat Pharma
02 1Temad Co
03 1LGM Pharma
04 1DKSH
05 1Jai Radhe Sales
06 1Faran Shimi Pharmaceutical
07 1Alkaloids Corporation
08 1Ax Pharmaceutical Corporation
09 1Biotechnica DWC
10 1Darmerica
11 2Fagron Group
12 1Guangzhou Tosun Pharmaceutical
13 1Inga Pharmaceuticals
14 1Kimyagaran
15 1Letco Medical
16 1Medisca
17 3Pcca
18 1Pharma Source Direct
19 2Recordati
20 2Saurav Chemicals
21 1Sichuan Renan Pharmaceutical
22 2Willow Birch Pharma
23 1elm-plastic GmbH
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01 1Algeria
02 1Canada
03 2China
04 1Germany
05 6India
06 3Iran
07 2Italy
08 2Netherlands
09 1Switzerland
10 7U.S.A
11 3United Kingdom
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01 1Active
02 6Inactive
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01 34Blank
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01 1231MF10018
02 33Blank
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01 1WC-0171
02 1WC-0171A3
03 1WC-301n
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01 120250324-211-J-1789
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01 210695-116
02 112711-7480
03 138779-0454
04 143235-0009
05 151552-0416
06 151927-0223
07 151927-0315
08 151927-1775
09 162991-1203
10 163570-030
11 171052-204
12 173377-253
13 176003-0850
14 182393-402
15 182429-528
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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
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
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
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A Pavased manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pavased, including repackagers and relabelers. The FDA regulates Pavased manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pavased API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Pavased supplier is an individual or a company that provides Pavased active pharmaceutical ingredient (API) or Pavased finished formulations upon request. The Pavased suppliers may include Pavased API manufacturers, exporters, distributors and traders.
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We have 23 companies offering Pavased
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