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01 1Aspen Pharmacare Holdings
02 1Strides Pharma Science
03 2AAIPharma Services Corp.
04 1Actavis Inc
05 6Adcock Ingram
06 1Algorithm
07 1Aurovitas Spain, Sau
08 1Barr Laboratories
09 1Be-Tabs Pharmaceuticals
10 1Centurion Laboratories
11 2Chartwell Pharmaceuticals llc
12 1Global Pharma Healthcare
13 1Glumex Pharmaceuticals Mfg. Pvt. Ltd
14 1Help Pharma Switzerland Ag
15 2Hexal AG
16 1Indo Pharma
17 1InterMed
18 2Kwality Pharmaceuticals
19 1MS Pharma
20 2Mepha Pharma
21 7Merck & Co
22 2Nordic Drugs
23 3ORIFARM GROUP AS
24 1PH HEALTH
25 1Padagis
26 1Pan Quimica Farmaceutica Sa
27 1Par Pharmaceutical
28 1Rising Pharmaceuticals Inc
29 3Sandoz B2B
30 1Sigmapharm Laboratories, LLC
31 1Specpharm
32 1Teofarma
33 1Teva Pharmaceutical Industries
34 1Viatris
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01 1Amiloride+Hydrochlorothiazide 5+50Mg 20 Joined' Oral Use
02 13TAB
03 3TABLET
04 11TABLET;ORAL
05 27Tablet
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01 3Allowed
02 6Approved
03 2Authorized
04 6DISCN
05 6Deregistered
06 12Generic
07 2Originator
08 2Prescription
09 5RX
10 1Suspensed
11 10Blank
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01 1AA-AMILZIDE
02 3AMILORIDE HYDROCHLORIDE
03 5AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
04 2Adco Retic
05 1Ameride
06 3Amiloretic
07 1Amiloretic H.S. Tablets
08 1Amilorida/Hidrochlorothiazida Aurovitas
09 1Amiloride Mylan
10 2Amiloride/Hydrochlorothiazide Sandoz
11 1Amyloferm
12 1Amyloferm Mite
13 1Betaretic
14 1Comilorid-Mepha
15 1Comilorid-Mepha gently
16 1Dezretic
17 1Diuzine
18 1Furosemide; Amiloride
19 1Grodurex
20 1HYDRO-RIDE
21 2MIDAMOR
22 1MODURETIC 5-50
23 1Midamor
24 4Moduretic
25 1Moduretic Mite
26 1Moduretic hs
27 1Normorix
28 2Normorix Mite
29 1Sandoz Co-Amilozide
30 1Servatrin
31 1Sparkal
32 1Sparkal Mite
33 1Spec-Co-Amiloride
34 7Blank
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01 2Canada
02 7India
03 1Italy
04 1Jordan
05 1Lebanon
06 1Norway
07 13South Africa
08 3Spain
09 12Sweden
10 3Switzerland
11 11USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Servatrin
Dosage Form : TAB
Dosage Strength : 2.5mg
Packaging : 30X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : India
Brand Name : Furosemide; Amiloride
Dosage Form : Tablet
Dosage Strength : 5MG; 40 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1991-07-19
Application Number : 73334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1988-05-10
Application Number : 71111
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1991-11-27
Application Number : 73357
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AMILORIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2015-08-07
Application Number : 204180
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : India
Amiloride; Hydrochlorothiazide
Brand Name :
Dosage Form : Tablet
Dosage Strength : 5MG; 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 10mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : MODURETIC 5-50
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 18201
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Amiloride; Hydrochlorothiazide
Brand Name : Moduretic
Dosage Form : Amiloride+Hydrochlorothiazide 5+50Mg 20 Joined' Oral Use
Dosage Strength : 20 CPR 5 mg + 50 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Generic
Registration Country : Jordan
Amiloride Hydrochloride; Hydrochlorothiazide
Brand Name :
Dosage Form : TABLET
Dosage Strength : 50MG; 5MG
Packaging : Pack Size - 1000 ,20
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Jordan
Regulatory Info :
Registration Country : Norway
Hydrochlorothiazide, Amiloride hydrochloride
Brand Name : Normorix Mite
Dosage Form : Tablet
Dosage Strength : 25 mg/2.5 mg
Packaging : Boks 100item
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : RX
Registration Country : USA
Brand Name : MIDAMOR
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 18200
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : HYDRO-RIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1990-12-25
Application Number : 70347
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1991-10-31
Application Number : 73209
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMILORIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2009-01-30
Application Number : 79133
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Packaging :
Approval Date : 1988-04-17
Application Number : 70795
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMILORIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1986-01-22
Application Number : 70346
Regulatory Info : RX
Registration Country : USA
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