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Approved Drug Products containing FOSINOPRIL SODIUM listed in the FDA Orange Book. Original Data : FDA Website

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01 RANBAXY LABS LTD (3)

02 SUN PHARM INDS LTD (2)

03 ACTAVIS LABS FL INC (3)

04 ANI PHARMS (4)

05 APOTEX INC (3)

06 AUROBINDO PHARMA (2)

07 AUROBINDO PHARMA LTD (3)

08 AVET LIFESCIENCES (2)

09 BRISTOL MYERS SQUIBB (5)

10 CHARTWELL RX (3)

11 INVAGEN PHARMS (5)

12 MYLAN (2)

13 PRINSTON INC (3)

14 SANDOZ (2)

15 TEVA (5)

16 UPSHER SMITH LABS (3)

17 WATSON LABS (6)

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01 TABLET;ORAL (56)

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01 DISCN (32)

02 RX (24)

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01 FOSINOPRIL SODIUM (33)

02 FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE (18)

03 MONOPRIL (3)

04 MONOPRIL-HCT (2)

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01 No (51)

02 Yes (5)

URL Supplier Web Content
TABLET;ORAL
10MG
2004-04-23
76580
FOSINOPRIL SODIUM
DISCN
No
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TABLET;ORAL
20MG
2004-04-23
76580
FOSINOPRIL SODIUM
DISCN
No
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TABLET;ORAL
40MG
2004-04-23
76580
FOSINOPRIL SODIUM
DISCN
No
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TABLET;ORAL
10MG;12.5MG
2004-12-17
76739
FOSINOPRIL SODIUM AND ...
DISCN
No
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TABLET;ORAL
20MG;12.5MG
2004-12-17
76739
FOSINOPRIL SODIUM AND ...
DISCN
No
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TABLET;ORAL
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1991-05-16
19915
MONOPRIL
DISCN
Yes
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TABLET;ORAL
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1991-05-16
19915
MONOPRIL
DISCN
Yes
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TABLET;ORAL
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1995-03-28
19915
MONOPRIL
DISCN
Yes
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TABLET;ORAL
20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1994-11-30
20286
MONOPRIL-HCT
DISCN
Yes
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TABLET;ORAL
10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1994-11-30
20286
MONOPRIL-HCT
DISCN
Yes
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