Hydrochlorothiazide

Product NDC

60760-413

11-digit product format

607600413

Labeler code

60760

Product ID

60760-413_7b207415-b031-9ab7-e053-2a91aa0a1902

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA084325

Marketing category

ANDA

Marketing start

2007-05-01

Marketing end

2020-06-30

Substance

HYDROCHLOROTHIAZIDE

Active strength

25 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