DYAZIDE

Product NDC

65084-135

11-digit product format

650840135

Labeler code

65084

Product ID

65084-135_a0053182-dd25-4095-baa2-6683b4cd7b95

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydrochlorothiazide and triamterene

Dosage form

CAPSULE

Route

ORAL

Labeler

Mckesson Rxpak Inc

Application

NDA016042

Marketing category

NDA

Marketing start

1994-03-30

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE; TRIAMTERENE

Active strength

25 mg/1; mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record