Triamterene hydrochlorothiazide

Product NDC

0781-5067

11-digit product format

007815067

Labeler code

0781

Product ID

0781-5067_2b550e14-4651-459c-b523-ee54f97fcb49

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Triamterene and hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA072011

Marketing category

ANDA

Marketing start

2017-04-20

Marketing end

2020-09-30

Substance

TRIAMTERENE; HYDROCHLOROTHIAZIDE

Active strength

75 mg/1; mg/1

Pharmacologic classes

Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record