Hydrochlorothiazide

Product NDC

68645-511

11-digit product format

686450511

Labeler code

68645

Product ID

68645-511_50e452b5-c243-480e-84ec-b63ca5b2f67c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA083177

Marketing category

ANDA

Marketing start

1980-01-07

Marketing end

2020-05-31

Substance

HYDROCHLOROTHIAZIDE

Active strength

50 mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record