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01 1Azure Pharmaceuticals Ltd

02 1Bristol Laboratories Ltd

03 3Bristol Myers Squibb

04 3Central Procurement & Supplies Unit

05 1Cosmos

06 2Crescent Pharma

07 2Evolan Pharma AB

08 2ExtractumPharma Co. Ltd

09 2Impax Laboratories

10 2Ipca Laboratories

11 6Karo Pharma

12 2Natco Pharma

13 2ORIFARM GROUP AS

14 1P & D Pharmaceuticals Limited

15 5Pfizer Inc

16 1RELIANCE FORMULATION PVT. LTD

17 2Teva Pharmaceutical Industries

18 1Viatris

19 2Wockhardt UK

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PharmaCompass

01

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2018-02-13

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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02

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE

Brand Name : NATURETIN-2.5

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12164

Regulatory Info : DISCN

Registration Country : USA

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03

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE

Brand Name : NATURETIN-5

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12164

Regulatory Info : DISCN

Registration Country : USA

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04

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE

Brand Name : NATURETIN-10

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12164

Regulatory Info : DISCN

Registration Country : USA

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05

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : BENDURIC

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Kenya

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06

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2019-06-17

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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07

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date : 2019-06-17

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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08

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;40MG

Packaging :

Approval Date : 2007-03-30

Application Number : 77833

Regulatory Info : DISCN

Registration Country : USA

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09

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;80MG

Packaging :

Approval Date : 2007-03-30

Application Number : 77833

Regulatory Info : DISCN

Registration Country : USA

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10

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name :

Dosage Form : TABLET

Dosage Strength : 2.5MG

Packaging :

Approval Date :

Application Number : 12164

Regulatory Info : Generic CTD, BE

Registration Country : India

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11

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name :

Dosage Form : TABLET

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number : 12164

Regulatory Info : Generic CTD, BE

Registration Country : India

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12

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;40MG

Packaging :

Approval Date : 2008-02-15

Application Number : 78688

Regulatory Info : DISCN

Registration Country : USA

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13

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;80MG

Packaging :

Approval Date : 2008-02-15

Application Number : 78688

Regulatory Info : DISCN

Registration Country : USA

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14

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : CORZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1983-05-25

Application Number : 18647

Regulatory Info : DISCN

Registration Country : USA

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15

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

BENDROFLUMETHIAZIDE; NADOLOL

Brand Name : CORZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1983-05-25

Application Number : 18647

Regulatory Info : DISCN

Registration Country : USA

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16

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name :

Dosage Form : Tablet

Dosage Strength : 2.5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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17

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date : 2006-08-18

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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18

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2012-07-16

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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19

P & D Pharmaceuticals Limited

Country
ASPEN
Not Confirmed
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P & D Pharmaceuticals Limited

Country
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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date : 2013-05-27

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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20

Central Procurement & Supplies Unit

Country
ASPEN
Not Confirmed
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Central Procurement & Supplies Unit

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ASPEN
Not Confirmed

Bendroflumethiazide

Brand Name : Bendroflumethiazide

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date : 2020-02-14

Application Number :

Regulatory Info : Invalid

Registration Country : Malta

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