Hydrochlorothiazide

Product NDC

0615-1358

11-digit product format

006151358

Labeler code

0615

Product ID

0615-1358_96e5457c-c9e8-47f9-bcec-a530cf80969a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

NDA020504

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1996-12-27

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

13 mg/1

Pharmacologic classes

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