Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 5Sanofi
02 1Acella Pharmaceuticals
03 2Alcon Inc
04 1Apotex Inc
05 1Brooks laboratories Limited
06 2Epic Pharma. LLC.
07 1Farmak JSC
08 1Flagship Biotech International Pvt. Ltd
09 1Gen-Eye
10 2KVK.Tech
11 1Laboratoires Alcon SA
12 1MEDIMETRIKS PHARMS
13 2Medius AG
14 1National Pharma
15 8Novartis Pharmaceuticals Corporation
16 1PRO.MED.CS Praha
17 3S.A. Alcon-Couvreur N.V.
18 2SA Alcon Couvreur NV
19 1Sandoz B2B
20 1ScieGen Pharmaceuticals
21 1Velpharm
22 1World Medicine
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01 1Betaxolol 20Mg 28 Combined Oral Use
02 1Betaxolol 5Mg/Ml 5Ml Solution Ophthalmic Use
03 1EYE DROPS
04 1EYE DROPS, SOLUTION
05 1EYE DROPS, SUSPENSION
06 1EYE DROPS, SUSPENSION IN SINGLE-DOSE CONTAINERS
07 1Eye Drop
08 1Eye Drops
09 1Eye drops, resolution
10 2Eye drops, suspension
11 1Eye/Ear Drop
12 1Film Coated Tablet
13 2Gtt Opht
14 4OPD
15 5SOLUTION/DROPS;OPHTHALMIC
16 1SUSPENSION
17 2SUSPENSION/DROPS;OPHTHALMIC
18 8TABLET;ORAL
19 2Tablet
20 3Blank
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01 7DISCN
02 2Generic
03 3Originator
04 1Prescription
05 8RX
06 19Blank
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01 1BETAKSIL
02 8BETAXOLOL HYDROCHLORIDE
03 1BETOPTIC
04 1BETOPTIC PILO
05 2BETOPTIC S
06 1Betaxolol PMCS
07 1Betaxolol Velpharm
08 1Betoftan
09 7Betoptic
10 6Betoptic S
11 1Betoptic S 0.25% Ophthalmic Suspension
12 1Betoptic S Single Dose
13 2KERLEDEX
14 2KERLONE
15 1Kerlon
16 1Loxoptic
17 3Blank
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01 3Australia
02 1Canada
03 1Czech Republic
04 3India
05 2Italy
06 3Norway
07 1Russia
08 4South Africa
09 3Sweden
10 2Switzerland
11 1Turkey
12 15USA
13 1Ukraine
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KERLONE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1989-10-27
Application Number : 19507
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KERLONE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1989-10-27
Application Number : 19507
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE
Brand Name : KERLEDEX
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG;12.5MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19807
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE
Brand Name : KERLEDEX
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;12.5MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19807
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Kerlon
Dosage Form : Betaxolol 20Mg 28 Combined Oral Use
Dosage Strength : 28 cpr riv 20 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 2009-11-16
Application Number : 78694
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BETAXOLOL HYDROCHLORIDE; PILOCARPINE HYDROCHLORIDE
Brand Name : BETOPTIC PILO
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.25% BASE;1.75%
Packaging :
Approval Date : 1997-04-17
Application Number : 20619
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 2000-09-28
Application Number : 75446
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 1999-10-22
Application Number : 75541
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 1999-10-22
Application Number : 75541
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Eye Drops
Dosage Strength : 0.25% W/V
Packaging : 2.5ml/5ml/10/15ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2008-06-27
Application Number : 78962
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 2008-06-27
Application Number : 78962
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 2001-04-12
Application Number : 75630
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETOPTIC S
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.25% BASE
Packaging :
Approval Date : 1989-12-29
Application Number : 19845
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETOPTIC
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 1985-08-30
Application Number : 19270
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 2000-06-30
Application Number : 75386
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Betoptic
Dosage Form : EYE DROPS, SOLUTION
Dosage Strength : 5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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Regulatory Info :
Registration Country : Sweden
Brand Name : Betoptic S
Dosage Form : EYE DROPS, SUSPENSION
Dosage Strength : 2.5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Betoptic S
Dosage Form : EYE DROPS, SUSPENSION IN SINGLE-DOSE CONTAINERS
Dosage Strength : 2.5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF