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01 3ACTAVIS LABS FL INC

02 4ANI PHARMS

03 3APOTEX INC

04 2AUROBINDO PHARMA

05 3AUROBINDO PHARMA LTD

06 2AVET LIFESCIENCES

07 5BRISTOL MYERS SQUIBB

08 3CHARTWELL RX

09 5INVAGEN PHARMS

10 2MYLAN

11 3PRINSTON INC

12 3RANBAXY LABS LTD

13 2SANDOZ

14 2SUN PHARM INDS LTD

15 5TEVA

16 3UPSHER SMITH LABS

17 6WATSON LABS

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PharmaCompass

01

Antibody Engineering
Not Confirmed
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Antibody Engineering
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-05-16

Application Number : 19915

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Antibody Engineering
Not Confirmed
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Antibody Engineering
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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-05-16

Application Number : 19915

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

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Dosage Strength : 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-03-28

Application Number : 19915

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

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Dosage Strength : 20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1994-11-30

Application Number : 20286

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Antibody Engineering
Not Confirmed
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Antibody Engineering
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**

Approval Date : 1994-11-30

Application Number : 20286

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2003-11-25

Application Number : 76139

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Approval Date : 2003-11-25

Application Number : 76139

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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08

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Approval Date : 2003-11-25

Application Number : 76139

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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09

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2004-10-08

Application Number : 76188

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Antibody Engineering
Not Confirmed
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arrow
Antibody Engineering
Not Confirmed

FOSINOPRIL SODIUM

Brand Name : FOSINOPRIL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Approval Date : 2004-10-08

Application Number : 76188

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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