Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1Neuland Laboratories
03 1Arevipharma
04 1Cambrex Corporation
05 1Erregierre SpA
06 1Heumann
07 1Siegfried AG
08 1Sifavitor srl
09 2Blank
01 1SOTALOL HCI
02 2SOTALOL HCL
03 6SOTALOL HYDROCHLORIDE
04 1SOTALOL HYDROCHLORIDE USP
01 2Germany
02 1India
03 2Italy
04 1Spain
05 1Switzerland
06 1U.S.A
07 2Blank
01 4Active
02 6Inactive
01 2Complete
02 8Blank
GDUFA
DMF Review : Complete
Rev. Date : 2021-06-22
Pay. Date : 2021-06-16
DMF Number : 13992
Submission : 1999-02-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-06-27
Pay. Date : 2014-06-23
DMF Number : 14951
Submission : 2000-07-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23752
Submission : 2010-04-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12273
Submission : 1996-12-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13083
Submission : 1998-07-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13186
Submission : 1998-09-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3721
Submission : 1980-02-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14841
Submission : 2000-04-20
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11887
Submission : 1996-03-06
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3754
Submission : 1980-03-12
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Sotalol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sotalol Hydrochloride, including repackagers and relabelers. The FDA regulates Sotalol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sotalol 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 Sotalol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sotalol Hydrochloride supplier is an individual or a company that provides Sotalol Hydrochloride active pharmaceutical ingredient (API) or Sotalol Hydrochloride finished formulations upon request. The Sotalol Hydrochloride suppliers may include Sotalol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sotalol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sotalol Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Sotalol Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Sotalol Hydrochloride DMFs exist exist since differing nations have different regulations, such as Sotalol Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sotalol Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Sotalol Hydrochloride USDMF includes data on Sotalol Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sotalol Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sotalol Hydrochloride suppliers with USDMF on PharmaCompass.
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