Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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01 1Polpharma
02 1LGM Pharma
03 1Jai Radhe Sales
04 1Century Pharmaceuticals
05 1Shandong Loncom Pharmaceutical
06 1AASraw Biochemical Technology Co., Ltd
07 1Alembic Pharmaceuticals Limited
08 1Ax Pharmaceutical Corporation
09 2Chromo Laboratories
10 1Darmerica
11 1Guangzhou Tosun Pharmaceutical
12 1Hangzhou Longshine Bio-Tech
13 1Hangzhou Think Chemical Co.Ltd
14 1Letco Medical
15 2Macleods Pharmaceuticals Limited
16 1Phalanx Labs
17 1Pharma Source Direct
18 1Raks Pharma
19 1Rakshit Drugs
20 1Remedy Labs
21 2SMS Pharmaceuticals
22 1Synaptics Labs
23 1Tianish Laboratories
24 1Ultratech India Ltd.,
25 1Unipex
26 1Viatris
27 3Willow Birch Pharma
28 1Xian Tian Guangyuan Biotech
29 1Zhejiang Bamboo Pharmaceuticals
30 1Blank
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01 1Canada
02 7China
03 1France
04 16India
05 1Poland
06 8U.S.A
07 1Blank
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01 6Active
02 29Blank
01 5Valid
02 30Blank
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01 1231MF10080
02 1301MF10002
03 33Blank
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01 1WC-0079A1
02 1WC-0079a
03 1WC-0082
04 1WC-0317
05 1WC-0317A2
06 1WC-0373
07 1WC-0373A4
08 1WC-257
09 27Blank
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01 120180222-211-J-181
02 120181028-211-J-269
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01 110695-120
02 110695-122
03 110695-123
04 112658-0463
05 133342-504
06 133342-604
07 147621-303
08 152562-004
09 162991-3167
10 167835-0014
11 171052-642
12 173377-007
13 181999-0008
14 182393-304
15 21Blank
01 35Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-15
Pay. Date : 2015-08-21
DMF Number : 25174
Submission : 2011-08-02
Status : Active
Type : II
Certificate Number : CEP 2014-106 - Rev 02
Issue Date : 2024-05-29
Type : Chemical
Substance Number : 2782
Status : Valid
Registration Number : 231MF10080
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2019-04-03
Latest Date of Registration :
NDC Package Code : 12658-0463
Start Marketing Date : 2003-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2018-10-28
Registration Number : 20181028-211-J-269
Manufacturer Name : Pharmaceutical Works Polpharma S.A.
Manufacturer Address : 19. Pelplinska Str, 83-200 Starogard Gdanski, Poland
Available Reg Filing : ASMF, CN, CA |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-13
Pay. Date : 2013-07-10
DMF Number : 25795
Submission : 2012-04-09
Status : Active
Type : II
Certificate Number : R1-CEP 2015-207 - Rev 00
Issue Date : 2021-09-21
Type : Chemical
Substance Number : 2782
Status : Valid
Date of Issue : 2020-07-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0079A1
Address of the Firm :
NDC Package Code : 33342-504
Start Marketing Date : 2016-02-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-02-20
Pay. Date : 2014-12-24
DMF Number : 28900
Submission : 2014-12-31
Status : Active
Type : II
Certificate Number : R1-CEP 2015-095 - Rev 01
Issue Date : 2023-06-26
Type : Chemical
Substance Number : 2782
Status : Valid
Registration Number : 301MF10002
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2019-05-08
Latest Date of Registration :
Date of Issue : 2022-06-17
Valid Till : 2025-07-02
Written Confirmation Number : WC-0082
Address of the Firm :
Registrant Name : M-Peak Korea Co., Ltd.
Registration Date : 2018-02-22
Registration Number : 20180222-211-J-181
Manufacturer Name : Alembic Pharmaceuticals Limited (API Unit-III)
Manufacturer Address : Plot No. 842-843, Taluka-Padra, City : Karakhadi - 391 450, District-Vadodara Gujarat State, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33220
Submission : 2019-03-07
Status : Active
Type : II
Date of Issue : 2022-02-02
Valid Till : 2024-06-07
Written Confirmation Number : WC-0317
Address of the Firm :
NDC Package Code : 52562-004
Start Marketing Date : 2020-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32908
Submission : 2018-09-20
Status : Active
Type : II
Certificate Number : CEP 2018-202 - Rev 01
Issue Date : 2024-04-04
Type : Chemical
Substance Number : 2782
Status : Valid
Date of Issue : 2022-07-08
Valid Till : 2025-07-21
Written Confirmation Number : WC-0373
Address of the Firm :
NDC Package Code : 67835-0014
Start Marketing Date : 2018-03-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-01-05
Pay. Date : 2016-10-03
DMF Number : 30804
Submission : 2016-10-27
Status : Active
Type : II
NDC Package Code : 47621-303
Start Marketing Date : 2017-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Vardenafil Hydrochloride 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 Vardenafil Hydrochloride manufacturer or Vardenafil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vardenafil Hydrochloride manufacturer or Vardenafil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Vardenafil Hydrochloride API Price utilized in the formulation of products. Vardenafil Hydrochloride API Price is not always fixed or binding as the Vardenafil Hydrochloride Price is obtained through a variety of data sources. The Vardenafil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vardenafil HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vardenafil HCl, including repackagers and relabelers. The FDA regulates Vardenafil HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vardenafil HCl 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 Vardenafil HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vardenafil HCl supplier is an individual or a company that provides Vardenafil HCl active pharmaceutical ingredient (API) or Vardenafil HCl finished formulations upon request. The Vardenafil HCl suppliers may include Vardenafil HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Vardenafil HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 29 companies offering Vardenafil HCl
Get in contact with the supplier of your choice: