Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Reset all filters
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 1Chromo Laboratories
10 1Darmerica
11 1Guangzhou Tosun Pharmaceutical
12 1Hangzhou Longshine Bio-Tech
13 1Hangzhou Think Chemical Co.Ltd
14 1Letco Medical
15 1Macleods Pharmaceuticals Limited
16 1Maithili Life Sciences
17 1Phalanx Labs
18 1Pharma Source Direct
19 1Raks Pharma
20 1Rakshit Drugs
21 1Remedy Labs
22 1SMS Pharmaceuticals
23 1Synaptics Labs
24 1Tianish Laboratories
25 1Unipex
26 1Viatris
27 3Willow Birch Pharma
28 1Xian Tian Guangyuan Biotech
29 1Zhejiang Bamboo Pharmaceuticals
30 3Blank
Reset all filters
01 1Canada
02 7China
03 1France
04 13India
05 1Poland
06 8U.S.A
07 3Blank
Reset all filters
01 6Active
02 28Blank
01 5Valid
02 29Blank
Reset all filters
01 1231MF10080
02 1301MF10002
03 32Blank
Reset all filters
01 1WC-0079
02 1WC-0317
03 32Blank
Reset all filters
01 120180222-211-J-181
02 120181028-211-J-269
03 32Blank
Reset all filters
01 210695-120
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 182053-005
15 182393-304
16 185411-116
17 17Blank
01 34Blank
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 : Zakłady Farmaceutyczne Polpharma SA
Manufacturer Address : ul. Peplińska 19, 83-200 Starogard Gdański, 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 : N/A
Rev. Date :
Pay. Date :
DMF Number : 32908
Submission : 2018-09-20
Status : Active
Type : II
Certificate Number : CEP 2018-202 - Rev 02
Issue Date : 2025-05-13
Type : Chemical
Substance Number : 2782
Status : Valid
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 : 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 : 2022-09-07
Valid Till : 2025-07-02
Written Confirmation Number : WC-0079
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 :
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 : 2024-07-06
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 : 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
90
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 STAXYN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of STAXYN, including repackagers and relabelers. The FDA regulates STAXYN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. STAXYN 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 STAXYN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A STAXYN supplier is an individual or a company that provides STAXYN active pharmaceutical ingredient (API) or STAXYN finished formulations upon request. The STAXYN suppliers may include STAXYN API manufacturers, exporters, distributors and traders.
click here to find a list of STAXYN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 29 companies offering STAXYN
Get in contact with the supplier of your choice: