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 3RANBAXY LABORATORIES LIMITED
19 2SANIS HEALTH INC
20 2Sandoz B2B
21 2Sun Pharmaceutical Industries Limited
22 10Teva Pharmaceutical Industries
23 3Upsher-Smith Laboratories
24 8Viatris
25 2Zentiva
26 10Blank
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 16TABLET
06 56TABLET;ORAL
07 2Tabl
08 12Tablet
09 11Tablets
10 4tablet
01 32DISCN
02 3Generic
03 2Generic BE- Available
04 3Originator
05 8Prescription
06 24RX
07 50Blank
01 2APO-FOSINOPRIL
02 2APO-Fosinopril
03 1Actavis Fosinopril 20Mg 28 Tablets Efg
04 1ELITEN
05 1Eliten
06 1FOSICOMBI
07 2FOSINOPRIL
08 1FOSINOPRIL AUROBINDO
09 1FOSINOPRIL DOC GENERIC
10 1FOSINOPRIL HYDROCHLOROTHIAZIDE DOC GENERIC
11 1FOSINOPRIL HYDROCHLOROTHIAZIDE MYLAN GENERICS
12 33FOSINOPRIL SODIUM
13 18FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
14 1FOSINOPRIL TEVA
15 1FOSINOPRIL ZENTIVA
16 1FOSIPRES
17 1Ficombi
18 5Finopril
19 4Finopril Idrocltiazide
20 2Fipres
21 1Fosinopril Aurobindo 20Mg 28 Tablets Efg
22 1Fosinopril Teva 20Mg 28 Tablets Efg
23 2Fosinopril-HCT-Mepha
24 1Fosinopril/Hydrochlorothiazide Aurobindo 20/12.5Mg 28 Tablets Efg
25 1Fosinopril/Hydrochlorothiazide Teva 20/12.5Mg 28 Tablets Efg
26 1Fositens 20Mg 28 Tablets (Pvc/Pvdc Blister Opaque/
27 1Fositens 20Mg 28 Tablets (Transparent Pvc/Pvdc Blister/)
28 1Fositens Plus 20/12.5Mg 28 Tablets (Opaque)
29 1Fositens Plus 20/12.5Mg 28 Tablets (Transparent)
30 3MONOPRIL
31 2MONOPRIL-HCT
32 1Monace 10
33 1Monace 20
34 2Monopril
35 1Monozide
36 1Mylan Forsinopril 20
37 1Mylan Fosinopril 10
38 1Mylan Fosinopril 20
39 1Mylan Fosinopril 20Mg 28 Tablets Efg
40 2PMS-FOSINOPRIL
41 1TENSOGARD
42 1TENSOZIDE
43 2TEVA-FOSINOPRIL
44 1Tensogard
45 1Tensozide
46 3fosinopril Actavis
47 3fosinopril Medis
48 4Blank
01 4Australia
02 8Canada
03 2India
04 26Italy
05 2Jordan
06 6South Africa
07 10Spain
08 6Sweden
09 2Switzerland
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
Brand Name : FOSINOPRIL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 2004-10-15
Application Number : 76620
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 : 2004-10-15
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 : RX
Registration Country : USA
Brand Name : FOSINOPRIL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2005-05-17
Application Number : 76906
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 : 2005-05-17
Application Number : 76906
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 : 2005-05-17
Application Number : 76906
Regulatory Info : RX
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
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;12.5MG
Packaging :
Approval Date : 2005-09-28
Application Number : 76961
Regulatory Info : RX
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 : 2004-12-17
Application Number : 76739
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 : 2004-12-17
Application Number : 76739
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
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;12.5MG
Packaging :
Approval Date : 2006-07-05
Application Number : 76945
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 : 2006-07-05
Application Number : 76945
Regulatory Info : DISCN
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
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