Triamterene and Hydrochlorothiazide

Product NDC

68788-9792

11-digit product format

687889792

Labeler code

68788

Product ID

68788-9792_d8fc529b-9e8c-452f-901e-ead95fac09b8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Triamterene and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA071851

Marketing category

ANDA

Marketing start

2012-04-30

Marketing end

0000-00-00

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record