Orange Book product · Generic (ANDA)
HYDRO-RIDE
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
At a glance
Dec 25, 1990
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 25, 1990
36 yr ago
Today
Pharmaceutical detail
Active ingredient
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength
EQ 5MG ANHYDROUS;50MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 070347
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- —MODURETIC 5-50Brand (NDA)
NDA 018201 · MERCK
- 1991AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 073357 · CHARTWELL RX
- 1991AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 073209 · RISING
- 1991AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 073334 · WATSON LABS
- 1988AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071111 · BARR
- 1988AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070795 · TEVA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
