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01 1BARR
02 2CHARTWELL RX
03 1ENDO OPERATIONS
04 1MERCK
05 1PADAGIS US
06 1PAR PHARM
07 1RISING
08 1SIGMAPHARM LABS LLC
09 1TEVA
10 1WATSON LABS
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01 11TABLET;ORAL
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01 6DISCN
02 5RX
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01 3AMILORIDE HYDROCHLORIDE
02 5AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
03 1HYDRO-RIDE
04 1MIDAMOR
05 1MODURETIC 5-50
01 9No
02 2Yes
RLD : No
TE Code :
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1991-07-19
Application Number : 73334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1988-05-10
Application Number : 71111
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1991-11-27
Application Number : 73357
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18201
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : MIDAMOR
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1982-01-01
Application Number : 18200
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : HYDRO-RIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1990-12-25
Application Number : 70347
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1991-10-31
Application Number : 73209
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AMILORIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2009-01-30
Application Number : 79133
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG ANHYDROUS;50MG
Approval Date : 1988-04-17
Application Number : 70795
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Brand Name : AMILORIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1986-01-22
Application Number : 70346
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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