LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 4Polpharma
03 1HRV Pharma
04 1SNJ Labs
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01 18Active
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01 4Valid
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01 1227MF10206
02 1227MF10208
03 1229MF10116
04 1301MF10026
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01 1WC-0040
02 1WC-0057n
03 1WC-0066
04 1WC-0084
05 1WC-0104
06 1WC-0113
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01 120110902-170-I-9-08
02 120110902-170-I-9-08(1)
03 120110902-170-I-9-08(2)
04 120110902-170-I-9-08(4)
05 120120907-170-I-44-03
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10 120130117-170-I-185-05(6)
11 120130129-170-I-321-01
12 120130329-170-I-181-06
13 120130329-170-I-181-06(1)
14 120130329-170-I-181-06(2)
15 120130329-170-I-181-06(3)
16 120130329-170-I-181-06(4)
17 120130329-170-I-181-06(5)
18 120130329-170-I-181-06(6)
19 120130329-170-I-181-06(8)
20 120130329-170-I-181-06(9)
21 120130912-170-I-365-10
22 120130912-170-I-365-10(2)
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24 120131220-170-I-387-11
25 120141209-170-I-420-12
26 120150409-170-I-438-13
27 120150515-170-I-446-14
28 120150827-170-I-457-15
29 120160713-170-I-472-16
30 120160713-170-I-472-16(1)
31 120161124-170-I-496-17
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33 120170803-170-I-513-18
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35 120190530-170-I-277-19
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01 110695-119
02 610695-311
03 112658-0410
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05 117205-096
06 138779-2443
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08 150379-0007
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12 155111-061
13 162991-3127
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16 165129-1024
17 165267-103
18 165841-134
19 165862-383
20 165977-0008
21 165977-0095
22 366039-806
23 169056-501
24 171052-315
25 173377-321
26 184040-003
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-04-03
Pay. Date : 2013-05-21
DMF Number : 20581
Submission : 2007-06-06
Status : Active
Type : II
NDC Package Code : 12658-0410
Start Marketing Date : 1996-12-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2020-01-13
Registration Number : 20130117-170-I-185-05(6)
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19. Pelplinska Str, 83-200 Starogard Gdanski, Poland
Available Reg Filing : ASMF |
SNJ Labs: WHO-GMP certified API leader in India, specializing in bulk drugs & intermediates with unmatched expertise.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-31
Pay. Date : 2013-07-18
DMF Number : 20932
Submission : 2007-10-05
Status : Active
Type : II
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm :
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
NDC Package Code : 12658-0492
Start Marketing Date : 1996-12-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2014-02-27
Registration Number : 20130117-170-I-185-05(4)
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19, Pelplinska Str. 83-200 Starogard Gdanski, Poland.
Available Reg Filing : ASMF |
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Registrant Name : Huons Co., Ltd.
Registration Date : 2013-04-10
Registration Number : 20130117-170-I-185-05(3)
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19, Pelplinska Str. 83-200 Starogard Gdanski, Poland
Available Reg Filing : ASMF |
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2013-01-17
Registration Number : 20130117-170-I-185-05
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19, Pelplinska Str. 83-200 Starogard Gdaski, Poland
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-02-21
Pay. Date : 2013-07-24
DMF Number : 23349
Submission : 2009-11-30
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-09-25
Pay. Date : 2023-09-20
DMF Number : 18172
Submission : 2005-03-04
Status : Active
Type : II
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
Registrant Name : The One Pharmtech Co., Ltd.
Registration Date : 2022-05-22
Registration Number : 20130329-170-I-181-06(9)
Manufacturer Name : Sun Pharmaceutical Industries Ltd.
Manufacturer Address : Plot No. 25, Phase -Ⅳ, GIDC Industrial Estate, Panoli -394 116, District Bharuch, Gujarat, India
19
PharmaCompass offers a list of Topiramate 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 Topiramate manufacturer or Topiramate supplier for your needs.
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A Topiramato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Topiramato, including repackagers and relabelers. The FDA regulates Topiramato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Topiramato 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 Topiramato supplier is an individual or a company that provides Topiramato active pharmaceutical ingredient (API) or Topiramato finished formulations upon request. The Topiramato suppliers may include Topiramato API manufacturers, exporters, distributors and traders.
click here to find a list of Topiramato suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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