Hydrochlorothiazide

Product NDC

68788-9867

11-digit product format

687889867

Labeler code

68788

Product ID

68788-9867_abf822a1-6864-444f-8066-6edd1b644d14

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

NDA020504

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2015-08-14

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

2018-12-31

Current FDA listing

Historical FDA.report record