Triamterene and Hydrochlorothiazide

Product NDC

53808-0804

11-digit product format

538080804

Labeler code

53808

Product ID

53808-0804_49974c21-8cf2-4f7f-b768-560e2fbe7b60

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

TRIAMTERENE AND HYDROCHLOROTHIAZIDE

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA071851

Marketing category

ANDA

Marketing start

2009-07-01

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

2017-12-31

Current FDA listing

Historical FDA.report record