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Approved Drug Products containing NCGC00024443-02 listed in the FDA Orange Book. Original Data : FDA Website

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01 BARR (1)

02 CHARTWELL RX (2)

03 MERCK (1)

04 PADAGIS US (1)

05 PAR PHARM (2)

06 RISING (1)

07 SIGMAPHARM LABS LLC (1)

08 TEVA (1)

09 WATSON LABS (1)

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01 TABLET;ORAL (11)

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01 DISCN (6)

02 RX (5)

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01 AMILORIDE HYDROCHLORIDE (3)

02 AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (5)

03 HYDRO-RIDE (1)

04 MIDAMOR (1)

05 MODURETIC 5-50 (1)

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01 No (9)

02 Yes (2)

URL Supplier Web Content
TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1991-07-19
73334
AMILORIDE HYDROCHLORID...
DISCN
No
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1988-05-10
71111
AMILORIDE HYDROCHLORID...
RX
No
AB
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1991-11-27
73357
AMILORIDE HYDROCHLORID...
DISCN
No
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
18201
MODURETIC 5-50
DISCN
Yes
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TABLET;ORAL
5MG
1982-01-01
18200
MIDAMOR
RX
Yes
AB
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TABLET;ORAL
5MG
1986-01-22
70346
AMILORIDE HYDROCHLORID...
RX
No
AB
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1990-12-25
70347
HYDRO-RIDE
DISCN
No
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1991-10-31
73209
AMILORIDE HYDROCHLORID...
RX
No
AB
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TABLET;ORAL
5MG
2009-01-30
79133
AMILORIDE HYDROCHLORID...
RX
No
AB
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TABLET;ORAL
EQ 5MG ANHYDROUS;50MG
1988-04-17
70795
AMILORIDE HYDROCHLORID...
DISCN
No
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