Triamterene hydrochlorothiazide

Product NDC

68001-215

11-digit product format

680010215

Labeler code

68001

Product ID

68001-215_37fb70dd-3d5f-4dc0-9cd9-fe1ae9419322

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Triamterene and hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

BluePoint Laboratories

Application

ANDA072011

Marketing category

ANDA

Marketing start

2014-02-26

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record