01 4ANI Pharmaceuticals Inc
02 9Actavis Inc
03 2Alphapharm PTY Ltd
04 7Apotex Inc
05 11Aurobindo Pharma Limited
06 2Aurovitas Spain, Sau
07 2Avet Pharmaceuticals
08 2Bausch Health
09 9Bristol Myers Squibb
10 3Chartwell Pharmaceuticals llc
11 4DOC Generici
12 5InvaGen Pharmaceuticals Inc
13 2MS Pharma
14 1Medis ehff
15 5Menarini
16 1Mepha Pharma
17 3PHARMASWISS CESKA REPUBL.S.R.O
18 3PHARMASWISS CESKA REPUBLIKA SRO
19 2Pharmascience Inc.
20 3Prinston
21 2SANIS HEALTH INC
22 2Sandoz B2B
23 5Sun Pharmaceutical Industries Limited
24 12Teva Pharmaceutical Industries
25 3Upsher-Smith Laboratories
26 8Viatris
27 2Zentiva
01 1Fosinopril 10Mg 28 Combined Oral Use
02 8Fosinopril 20Mg 14 Joined' Oral Use
03 6Fosinopril+Hydrochlorothiazide+12,520 Mg 14 Joined' Oral Use
04 6TAB
05 10TABLET
06 56TABLET;ORAL
07 12Tablet
08 11Tablets
09 4tablet
01 1Allowed
02 4Authorized
03 3Cancelled
04 35DISCN
05 2Deregistered
06 3Generic
07 2Generic BE- Available
08 3Originator
09 8Prescription
10 21RX
11 32Blank
01 2APO-FOSINOPRIL
02 2APO-Fosinopril
03 1ELITEN
04 1Eliten
05 1FOSICOMBI
06 2FOSINOPRIL
07 1FOSINOPRIL AUROBINDO
08 1FOSINOPRIL DOC GENERIC
09 1FOSINOPRIL HYDROCHLOROTHIAZIDE DOC GENERIC
10 1FOSINOPRIL HYDROCHLOROTHIAZIDE MYLAN GENERICS
11 33FOSINOPRIL SODIUM
12 18FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
13 1FOSINOPRIL TEVA
14 1FOSINOPRIL ZENTIVA
15 1FOSIPRES
16 1Ficombi
17 5Finopril
18 4Finopril Idrocltiazide
19 2Fipres
20 1Fosinopril /Hidroclorotiazida Teva
21 1Fosinopril Aurobindo
22 1Fosinopril Aurovitas
23 1Fosinopril Teva
24 1Fosinopril-HCT-Mepha
25 1Fosinopril/Hidroclorotiazida Aurovitas
26 1Fosinopril/Hydrochlorothiazide Medication
27 1Fositens
28 1Fositens Plus
29 3MONOPRIL
30 2MONOPRIL-HCT
31 1Monace 10
32 1Monace 20
33 2Monopril
34 1Monopril Comp
35 1Monozide
36 1Mylan Forsinopril 20
37 1Mylan Fosinopril 10
38 1Mylan Fosinopril 20
39 2PMS-FOSINOPRIL
40 1TENSOGARD
41 1TENSOZIDE
42 2TEVA-FOSINOPRIL
43 1Tensogard
44 1Tensozide
45 4Blank
01 4Australia
02 8Canada
03 2India
04 26Italy
05 2Jordan
06 6South Africa
07 7Spain
08 2Sweden
09 1Switzerland
10 56USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
