01 1Amsa Spa
02 1Archimica
03 3AstraZeneca
04 1COSMA S.p.A
05 1Erregierre SpA
06 2Ipca Laboratories
07 1J.B.Chemicals & Pharmaceuticals
08 2Kopran
09 1Recordati
10 1SIMS Srl
11 1SINTENOVO, S.A. DE C.V.
12 1Shanghai Ziyuan Pharmaceutical
13 1Syn-Tech Chem. & Pharm
14 1Teva Pharmaceutical Industries
15 1Viatris
16 1Wanbury Limited
17 1Zydus Lifesciences
18 8Blank
01 19ATENOLOL
02 1ATENOLOL ACETATE
03 2ATENOLOL BULK DRUG
04 7ATENOLOL USP
01 1China
02 7India
03 1Israel
04 6Italy
05 1Mexico
06 1Taiwan
07 1U.S.A
08 3United Kingdom
09 8Blank
01 6Active
02 23Inactive
01 5Complete
02 24Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7101
Submission : 1987-08-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6905
Submission : 1987-03-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6325
Submission : 1986-03-01
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-01-22
Pay. Date : 2024-01-17
DMF Number : 15037
Submission : 2000-09-08
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-06-14
Pay. Date : 2016-03-21
DMF Number : 24024
Submission : 2010-08-10
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-01-17
Pay. Date : 2018-09-06
DMF Number : 33007
Submission : 2018-07-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6979
Submission : 1987-05-05
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-11
Pay. Date : 2012-11-13
DMF Number : 6213
Submission : 1986-03-05
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-01
Pay. Date : 2016-03-22
DMF Number : 14210
Submission : 1999-06-14
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6921
Submission : 1987-04-10
Status : Inactive
Type : II
Portfolio PDF
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Corporate PDF
A Tenormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenormin, including repackagers and relabelers. The FDA regulates Tenormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenormin 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 Tenormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenormin supplier is an individual or a company that provides Tenormin active pharmaceutical ingredient (API) or Tenormin finished formulations upon request. The Tenormin suppliers may include Tenormin API manufacturers, exporters, distributors and traders.
click here to find a list of Tenormin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenormin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tenormin active pharmaceutical ingredient (API) in detail. Different forms of Tenormin DMFs exist exist since differing nations have different regulations, such as Tenormin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tenormin DMF submitted to regulatory agencies in the US is known as a USDMF. Tenormin USDMF includes data on Tenormin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tenormin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tenormin suppliers with USDMF on PharmaCompass.
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