Triamterene and Hydrochlorothiazide

Product NDC

68788-9494

11-digit product format

687889494

Labeler code

68788

Product ID

68788-9494_46452b1f-ffe3-4298-a1d2-eee4df46d9f2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Triamterene and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA071251

Marketing category

ANDA

Marketing start

2014-04-02

Marketing end

0000-00-00

Substance

TRIAMTERENE; HYDROCHLOROTHIAZIDE

Active strength

38 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

2017-12-31

Current FDA listing

Historical FDA.report record