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01 4ANI Pharmaceuticals Inc

02 15Actavis Inc

03 2Alphapharm PTY Ltd

04 7Apotex Inc

05 10Aurobindo Pharma Limited

06 2Avet Pharmaceuticals

07 8Bristol Myers Squibb

08 3Chartwell Pharmaceuticals llc

09 4DOC Generici

10 5InvaGen Pharmaceuticals Inc

11 2MS Pharma

12 5Menarini

13 2Mepha Pharma

14 3PHARMASWISS CESKA REPUBL.S.R.O

15 3PHARMASWISS CESKA REPUBLIKA SRO

16 2Pharmascience Inc.

17 3Prinston

18 2SANIS HEALTH INC

19 2Sandoz B2B

20 5Sun Pharmaceutical Industries Limited

21 10Teva Pharmaceutical Industries

22 3Upsher-Smith Laboratories

23 8Viatris

24 2Zentiva

25 10Blank

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PharmaCompass

01

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-10-15

Application Number : 76620

Regulatory Info : DISCN

Registration Country : USA

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02

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;12.5MG

Packaging :

Approval Date : 2004-12-03

Application Number : 76608

Regulatory Info : DISCN

Registration Country : USA

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03

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG;12.5MG

Packaging :

Approval Date : 2004-12-03

Application Number : 76608

Regulatory Info : DISCN

Registration Country : USA

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04

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : MONOPRIL

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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1991-05-16

Application Number : 19915

Regulatory Info : DISCN

Registration Country : USA

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05

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : MONOPRIL

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 : 1991-05-16

Application Number : 19915

Regulatory Info : DISCN

Registration Country : USA

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06

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : MONOPRIL

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 1995-03-28

Application Number : 19915

Regulatory Info : DISCN

Registration Country : USA

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07

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Brand Name : MONOPRIL-HCT

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-11-30

Application Number : 20286

Regulatory Info : DISCN

Registration Country : USA

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08

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Brand Name : MONOPRIL-HCT

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-11-30

Application Number : 20286

Regulatory Info : DISCN

Registration Country : USA

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09

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76483

Regulatory Info : RX

Registration Country : USA

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10

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76483

Regulatory Info : RX

Registration Country : USA

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11

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76483

Regulatory Info : RX

Registration Country : USA

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12

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76580

Regulatory Info : DISCN

Registration Country : USA

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13

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76580

Regulatory Info : DISCN

Registration Country : USA

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14

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2004-04-23

Application Number : 76580

Regulatory Info : DISCN

Registration Country : USA

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15

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2003-11-25

Application Number : 76139

Regulatory Info : RX

Registration Country : USA

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16

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2003-11-25

Application Number : 76139

Regulatory Info : RX

Registration Country : USA

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17

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2003-11-25

Application Number : 76139

Regulatory Info : RX

Registration Country : USA

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18

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-10-08

Application Number : 76188

Regulatory Info : DISCN

Registration Country : USA

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19

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2004-10-08

Application Number : 76188

Regulatory Info : DISCN

Registration Country : USA

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20

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2004-10-08

Application Number : 76188

Regulatory Info : DISCN

Registration Country : USA

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