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Summary Of Atenolol-API-Small Molecules
Download All File (.xls)
BASIC INFORMATION
Chemical Name
Atenolol
CAS No.
29122-68-7
Molecular Formula
C14H22N2O3
Innovator
Developer
Indication
Hypertension; Myocardial Infarction
Therapeutic Area
Cardiovascular Disease
Market Status
Launched
Approval Year
Patent Expiry
DETAILED ANALYSIS (TECHNICAL INFO/COMMERCIAL INFO/SUPPLIER INFO/BUYER INFO)
Technical Info
Industry Application
End Application
Route Of Synthesis
Technology
Mechanism Of Action
Commercial Info
Global Market Size(MT)
AI
Global Market Size(MT)
AI
0
Global Market Size(MUSD)
AI
Global Market Size(MUSD)
AI
0
Average Price(USD/KG.)
AI
Average Price(USD/KG.)
AI
0
US Drug Sales(MUSD)
FDF
US Drug Sales(MUSD)
FDF
0
UK Drug Sales
FDF
UK Drug Sales
FDF
0
Supplier Info
No. Of Supplier
No. Of Supplier
0
Supplying Volume
Supplying Volume
0
Supplier Certification
Supplier Certification
0
No. Of Supplier Country
No. Of Supplier Country
0
No. Of Supplier Email
No. Of Supplier Email
0
Buyer Info
No. Of Buyer
No. Of Buyer
0
Buying Volume
Buying Volume
0
Buyer Certification
Buyer Certification
0
No. Of Buyer Country
No. Of Buyer Country
0
No. Of Buyer Email
No. Of Buyer Email
0
REGULATORY INFO -ACTIVE INGREDIENTS (FILING/REGISTRATION/MARKET AUTHORIZATION)
North America
US-DMF
US-DMF
0
FDA-NDC
FDA-NDC
0
Europe
CEP/COS
CEP/COS
0
EU-API Registered
EU-API Registered
0
EU-Written Conf-India
EU-Written Conf-India
0
REACH Registered
REACH Registered
0
UK-MHRA
UK-MHRA
0
Asia
J-DMF
J-DMF
0
K-DMF
K-DMF
0
India Import Licence
India Import Licence
0
China-API Registered
China-API Registered
0
Egypt-API Registered
Egypt-API Registered
0
REGULATORY INFO - (FINISHED DOSAGE FORMS(FDF) FILING/REGISTRATION/MARKET AUTHORIZATION)
North America
US-ANDA
US-ANDA
0
Canada
Canada
0
Cuba
Cuba
0
Mexico
Mexico
0
US-Excipients
US-Excipients
0
US-Veterinary
US-Veterinary
0
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Europe
National Registered
Netherland
Netherland
0
United Kingdom
United Kingdom
0
Spain
Spain
0
Italy
Italy
0
France
France
0
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Centralised
Centralized Registered
Centralized Registered
0
Decentralised
Decentralized Registered
Decentralized Registered
0
Others
Veterinary Registered
Veterinary Registered
0
UK Parallel Import Licence
UK Parallel Import Licence
0
Oceania
Australia
Australia
0
New Zealand
New Zealand
0
Africa
Cameroon
Cameroon
0
Nigeria
Nigeria
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Ethopia
Ethopia
0
South Africa
South Africa
0
Tanzania
Tanzania
0
Ghana
Ghana
0
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Asia
Japan
Japan
0
South Korea
South Korea
0
Indonesia
Indonesia
0
Thailand
Thailand
0
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Srilanka
0
India Import License
India Import License
0
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Egypt
Egypt
0
Saudi Arabia
Saudi Arabia
0
Philippines
Philippines
0
Turkey
Turkey
0
Vietnam
Vietnam
0
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UAE
0
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South America
Brazil
Brazil
0
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Argentina
0
Colombia
Colombia
0
Ecuador
Ecuador
0
Peru
Peru
0
Bolivia
Bolivia
0
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REGULATORY INFO - (CLINICAL TRIAL/PATENT/CERTIFICATION/ACCREDITATION/WARNING/ALERT)
Clinical Trial
United States
United States
0
Europe
Europe
0
Japan
Japan
0
Canada
Canada
0
Korea
Korea
0
India
India
0
Australia & New Zealand
Australia & New Zealand
0
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Patent
US-Patent Expiry
US-Patent Expiry
0
Canada-Patent Expiry
Canada-Patent Expiry
0
US-Exclusivity
US-Exclusivity
0
US-SPC
US-SPC
0
US-PARA IV
US-PARA IV
0
US-Off Patent-No Generics
US-Off Patent-No Generics
0
US-Pharma Patent Disputes
US-Pharma Patent Disputes
0
Canada-Patent Data Protection
Canada-Patent Data Protection
0
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Certification/ Accreditation
US-FDA Certified Facility
US-FDA Certified Facility
0
EU-GMP Certified Facility
EU-GMP Certified Facility
0
Japan-PMDA Certified Facility
Japan-PMDA Certified Facility
0
Canada-Certified Facility
Canada-Certified Facility
0
India-CDSCO Certified Facility
India-CDSCO Certified Facility
0
India-WHO GMP Certified Facility
India-WHO GMP Certified Facility
0
India-PICS Approved Facility
India-PICS Approved Facility
0
UK Certified Facility
UK Certified Facility
0
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Warning/Alert
US-FDA Recall
US-FDA Recall
0
US-FDA Warning
US-FDA Warning
0
US-FDA Form 483
US-FDA Form 483
0
US-FDA Site Inspection
US-FDA Site Inspection
0
India-CDSCO Banned Drug
India-CDSCO Banned Drug
0
India-NPPA
India-NPPA
0
India-NLEM
India-NLEM
0
WHO-Essential Drug
WHO-Essential Drug
0
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REGULATORY INFO - (BIOSIMILAR FILING/REGISTRATION/MARKET AUTHORIZATION)
Biosimilar
United States
Canada
Argentina
Brazil
Europe
Australia
Japan
South korea
India
China
Malaysia
REGULATORY INFO - (AGROCHEMICALS FILING/REGISTRATION/MARKET AUTHORIZATION)
Agrochemicals
Europe
United Kingdom
Spain
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Malta
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