Hydrochlorothiazide

Product NDC

66267-107

11-digit product format

662670107

Labeler code

66267

Product ID

66267-107_9cae12dc-4a00-2247-e053-2995a90a7599

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA202556

Marketing category

ANDA

Marketing start

2013-04-10

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

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record