Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1LGM Pharma
03 1Seqens
04 1Chemische Fabrik Berg
05 1Moehs Iberica
06 1HRV Global Life Sciences
07 1Synthokem Labs
08 3TAPI Technology & API Services
09 1Abbott Laboratories
10 1Apotex Pharmachem
11 1Archimica
12 1Aurobindo Pharma Limited
13 1BASF Corp
14 3Bioindustria L.I.M. Spa
15 1CTX Lifesciences
16 1Catalent Pharma Solutions
17 1Cilag AG
18 1Enaltec Labs Private Limited
19 1Jubilant Generics
20 1Jubilant Pharmova
21 1Second Pharma Co
22 1Signa S.A. de C.V.
23 1Standard Chem. & Pharm. Co., Ltd
24 1Sumitomo Chemical
25 1Weihai Disu Pharmacuetical Co., Ltd.
26 1Zydus Lifesciences
27 3Blank
01 1Canada
02 3China
03 1France
04 1Germany
05 9India
06 3Israel
07 4Italy
08 1Japan
09 1Mexico
10 1Spain
11 1Switzerland
12 3U.S.A
13 4Blank
01 8Active
02 16Inactive
03 9Blank
01 1Suspended by EDQM Failure to CEP procedure
02 4Valid
03 28Blank
01 33Blank
01 1WC-0092
02 1WC-0097
03 1WC-0120
04 30Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37577
Submission : 2022-10-31
Status : Active
Type : II
NDC Package Code : 73435-029
Start Marketing Date : 2022-12-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10035
Submission : 1993-01-11
Status : Active
Type : II
Certificate Number : R1-CEP 2014-214 - Rev 00
Issue Date : 2022-02-08
Type : Chemical
Substance Number : 2021
Status : Valid
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-30
Pay. Date : 2012-11-13
DMF Number : 11300
Submission : 1995-01-16
Status : Active
Type : II
Certificate Number : R1-CEP 2007-207 - Rev 05
Issue Date : 2022-04-19
Type : Chemical
Substance Number : 2021
Status : Valid
Available Reg Filing : CA, ASMF |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13959
Submission : 1999-01-26
Status : Active
Type : II
Available Reg Filing : CA, ASMF |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13194
Submission : 1998-09-23
Status : Inactive
Type : II
Available Reg Filing : CA, ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-12-08
Pay. Date : 2022-10-21
DMF Number : 14916
Submission : 2000-06-12
Status : Active
Type : II
NDC Package Code : 63809-2740
Start Marketing Date : 2000-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Unimed Pharmaceutical Co., Ltd.
Registration Date : 2015-05-22
Registration Number : 20050831-48-B-131-04(2)
Manufacturer Name : Bioindustria LIMSpA_x000D_
Manufacturer Address : Via Giustizia 1-15064 FRESONARA(AL)-ITALY (Via De Ambrosiis 2-4-6-15067 NOVI LIGURE-Italy)
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20113
Submission : 2006-12-30
Status : Active
Type : II
Certificate Number : CEP 2007-092 - Rev 05
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 2021
Status : Valid
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0120
Address of the Firm :
NDC Package Code : 65862-205
Start Marketing Date : 2023-11-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21066
Submission : 2007-11-13
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-12-11
Pay. Date : 2014-04-04
DMF Number : 18268
Submission : 2005-04-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9157
Submission : 1991-06-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13166
Submission : 1998-09-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19480
Submission : 2006-05-25
Status : Inactive
Type : II
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-48-B-128-02
Manufacturer Name : Euticals SpA
Manufacturer Address : Viale Europa 5, I-21040 Origgio-Italy
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10319
Submission : 1993-06-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20025
Submission : 2006-10-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12649
Submission : 1997-09-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12424
Submission : 1997-03-17
Status : Inactive
Type : II
NDC Package Code : 63809-2740
Start Marketing Date : 2000-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Unimed Pharmaceutical Co., Ltd.
Registration Date : 2015-05-22
Registration Number : 20050831-48-B-131-04(2)
Manufacturer Name : Bioindustria LIMSpA_x000D_
Manufacturer Address : Via Giustizia 1-15064 FRESONARA(AL)-ITALY (Via De Ambrosiis 2-4-6-15067 NOVI LIGURE-Italy)
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12802
Submission : 1997-12-22
Status : Inactive
Type : II
NDC Package Code : 63809-2740
Start Marketing Date : 2000-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Unimed Pharmaceutical Co., Ltd.
Registration Date : 2015-05-22
Registration Number : 20050831-48-B-131-04(2)
Manufacturer Name : Bioindustria LIMSpA_x000D_
Manufacturer Address : Via Giustizia 1-15064 FRESONARA(AL)-ITALY (Via De Ambrosiis 2-4-6-15067 NOVI LIGURE-Italy)
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12244
Submission : 1996-11-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17605
Submission : 2004-08-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25829
Submission : 2012-03-24
Status : Inactive
Type : II
Date of Issue : 2022-06-24
Valid Till : 2025-07-02
Written Confirmation Number : WC-0097
Address of the Firm :
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 : 10054
Submission : 1993-01-21
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 : 12581
Submission : 1997-07-08
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 : 14532
Submission : 1999-11-15
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 : 19362
Submission : 2006-04-08
Status : Inactive
Type : II
Certificate Number : CEP 2022-409 - Rev 00
Issue Date : 2024-08-30
Type : Chemical
Substance Number : 2021
Status : Valid
A Terazosin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terazosin Hydrochloride, including repackagers and relabelers. The FDA regulates Terazosin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terazosin Hydrochloride 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 Terazosin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terazosin Hydrochloride supplier is an individual or a company that provides Terazosin Hydrochloride active pharmaceutical ingredient (API) or Terazosin Hydrochloride finished formulations upon request. The Terazosin Hydrochloride suppliers may include Terazosin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Terazosin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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