Hydrochlorothiazide

Product NDC

57237-199

11-digit product format

572370199

Labeler code

57237

Product ID

57237-199_6d3c9548-985d-4b01-9d3b-360f5abbdd79

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Citron Pharma LLC

Application

ANDA040780

Marketing category

ANDA

Marketing start

2007-07-20

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

50 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