Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1LGM Pharma
03 1Jai Radhe Sales
04 1CR Double-Crane Pharmaceuticals Co., Ltd
05 1CTX Lifesciences
06 1Cambrex Corporation
07 1Emcure Pharmaceuticals
08 1Euroasia Trans Continental
09 1F. Hoffmann-La Roche
10 1GLAND PHARMA LIMITED
11 1Guangzhou Tosun Pharmaceutical
12 1IDT Australia Limited
13 3NAKODA CHEMICALS LIMITED
14 1Osmopharm
15 1Regis Technologies
16 1Sneha Medicare Pvt Ltd
17 2TATEYAMA KASEI CO LTD
18 1Teva Pharmaceutical Industries
19 2Blank
01 1Australia
02 2China
03 9India
04 1Israel
05 2Japan
06 1Poland
07 2Switzerland
08 3U.S.A
09 2Blank
01 7Active
02 5Inactive
03 11Blank
01 6Valid
02 17Blank
01 1220MF10066
02 1224MF10018
03 1224MF10235
04 1306MF10013
05 19Blank
01 1WC-0018
02 1WC-0097
03 1WC-0226
04 20Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-30
Pay. Date : 2013-01-15
DMF Number : 10383
Submission : 1993-07-30
Status : Active
Type : II
Certificate Number : R1-CEP 2010-371 - Rev 02
Issue Date : 2020-08-04
Type : Chemical
Substance Number : 454
Status : Valid
Registration Number : 306MF10013
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2024-01-24
Latest Date of Registration :
NDC Package Code : 12658-0359
Start Marketing Date : 1982-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (40kg/40kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2020-10-19
Registration Number : 20201019-210-J-595
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19. Pelplinska Str, 83-200 Starogard Gdanski, Poland
Available Reg Filing : ASMF |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-17
Pay. Date : 2013-03-06
DMF Number : 20299
Submission : 2007-02-23
Status : Active
Type : II
Certificate Number : CEP 2018-203 - Rev 01
Issue Date : 2023-11-27
Type : Chemical
Substance Number : 454
Status : Valid
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm :
NDC Package Code : 14593-801
Start Marketing Date : 2008-06-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-03-15
Pay. Date : 2023-02-09
DMF Number : 37616
Submission : 2022-10-31
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-09
Pay. Date : 2012-12-10
DMF Number : 23014
Submission : 2009-07-31
Status : Active
Type : II
Certificate Number : R1-CEP 2010-073 - Rev 03
Issue Date : 2022-11-14
Type : Chemical
Substance Number : 454
Status : Valid
Date of Issue : 2022-06-24
Valid Till : 2025-07-02
Written Confirmation Number : WC-0097
Address of the Firm :
NDC Package Code : 42419-008
Start Marketing Date : 2009-01-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-19
Pay. Date : 2013-03-13
DMF Number : 12997
Submission : 1998-05-21
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-07
Pay. Date : 2013-01-31
DMF Number : 19763
Submission : 2006-08-24
Status : Active
Type : II
Certificate Number : R1-CEP 2001-387 - Rev 05
Issue Date : 2022-05-13
Type : Chemical
Substance Number : 454
Status : Valid
Registration Number : 220MF10066
Registrant's Address : Plot No. 64/A & 65/B, Phase-I, IDA, Jeedimetla, Hyderabad-500 055, Telangana State, India
Initial Date of Registration : 2008-02-25
Latest Date of Registration :
Date of Issue : 2022-06-06
Valid Till : 2025-06-02
Written Confirmation Number : WC-0018
Address of the Firm :
NDC Package Code : 67123-001
Start Marketing Date : 2006-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22420
Submission : 2009-01-22
Status : Active
Type : II
NDC Package Code : 12817-363
Start Marketing Date : 1956-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2561
Submission : 1975-08-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2833
Submission : 1977-01-12
Status : Inactive
Type : II
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 : 3443
Submission : 1979-02-02
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 : 3959
Submission : 1980-09-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4647
Submission : 1982-08-05
Status : Inactive
Type : II
Registration Number : 224MF10018
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2012-02-01
Latest Date of Registration :
Certificate Number : R1-CEP 2010-352 - Rev 01
Issue Date : 2022-05-13
Type : Chemical
Substance Number : 454
Status : Valid
NDC Package Code : 67123-001
Start Marketing Date : 2006-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2011-290 - Rev 01
Issue Date : 2022-05-13
Type : Chemical
Substance Number : 454
Status : Valid
NDC Package Code : 67123-001
Start Marketing Date : 2006-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Registration Number : 224MF10235
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2012-12-20
Latest Date of Registration :
A Carbinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbinib, including repackagers and relabelers. The FDA regulates Carbinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbinib 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 Carbinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carbinib supplier is an individual or a company that provides Carbinib active pharmaceutical ingredient (API) or Carbinib finished formulations upon request. The Carbinib suppliers may include Carbinib API manufacturers, exporters, distributors and traders.
click here to find a list of Carbinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 18 companies offering Carbinib
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