Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience
02 1Moehs Iberica
03 1Arevipharma
04 1Aurobindo Pharma Limited
05 1Chongqing Lummy Pharmaceutical
06 1CordenPharma
07 2Ipca Laboratories
08 1Medilux Laboratories
09 1Merck Group
10 1Micro Labs Limited
11 1Piramal Pharma Solutions
12 1Taiwan Biotech
13 1Unichem Laboratories Limited
01 6BISOPROLOL FUMARATE
02 1BISOPROLOL FUMARATE 2:1
03 6BISOPROLOL FUMARATE USP
04 1BISOPROLOL FUMARATE USP (PROCESS II)
01 2China
02 3Germany
03 7India
04 1Spain
05 1U.S.A
01 12Active
02 2Inactive
01 7Complete
02 7Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35650
Submission : 2021-02-16
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-09-11
Pay. Date : 2015-09-04
DMF Number : 15083
Submission : 2000-10-10
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-12-18
Pay. Date : 2013-08-02
DMF Number : 23241
Submission : 2009-11-02
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-03-01
Pay. Date : 2019-01-28
DMF Number : 18781
Submission : 2005-09-12
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-02-08
Pay. Date : 2017-10-10
DMF Number : 13910
Submission : 1998-12-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-11-01
Pay. Date : 2013-08-30
DMF Number : 26667
Submission : 2013-08-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8024
Submission : 1989-04-12
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-11-13
Pay. Date : 2019-09-27
DMF Number : 29123
Submission : 2015-03-26
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20120
Submission : 2006-12-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16398
Submission : 2003-01-29
Status : Active
Type : II
A Bisoprolol Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bisoprolol Fumarate, including repackagers and relabelers. The FDA regulates Bisoprolol Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bisoprolol Fumarate 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 Bisoprolol Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bisoprolol Fumarate supplier is an individual or a company that provides Bisoprolol Fumarate active pharmaceutical ingredient (API) or Bisoprolol Fumarate finished formulations upon request. The Bisoprolol Fumarate suppliers may include Bisoprolol Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Bisoprolol Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bisoprolol Fumarate DMF (Drug Master File) is a document detailing the whole manufacturing process of Bisoprolol Fumarate active pharmaceutical ingredient (API) in detail. Different forms of Bisoprolol Fumarate DMFs exist exist since differing nations have different regulations, such as Bisoprolol Fumarate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Bisoprolol Fumarate DMF submitted to regulatory agencies in the US is known as a USDMF. Bisoprolol Fumarate USDMF includes data on Bisoprolol Fumarate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Bisoprolol Fumarate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Bisoprolol Fumarate suppliers with USDMF on PharmaCompass.
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