NDCFind

Hydrochlorothiazide 82804-0031

Product NDC

82804-0031
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 15, 2008
Listing Expires
December 31, 2026
Application
ANDA040907
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Active Ingredients

IngredientStrength
Hydrochlorothiazide50 mg/1

Drug Class

Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]

Packaging Options(3)

30 TABLET in 1 BOTTLE (82804-031-30)

60 TABLET in 1 BOTTLE (82804-031-60)

90 TABLET in 1 BOTTLE (82804-031-90)