Hydrochlorothiazide

Product NDC

63629-6377

11-digit product format

636296377

Labeler code

63629

Product ID

63629-6377_e0ab2a3a-f05f-4071-a7c5-8ddf1ba09d7c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA083177

Marketing category

ANDA

Marketing start

1973-01-12

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

25 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record