Orange Book product · Generic (ANDA)
HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE
At a glance
Jan 19, 2010
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 19, 2010
16 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCHLOROTHIAZIDE
Strength
12.5MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 090510
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCHLOROTHIAZIDE
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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.
