Hydrochlorothiazide

Product NDC

70518-0667

11-digit product format

705180667

Labeler code

70518

Product ID

70518-0667_8a9df3a5-e7ad-5da2-e053-2995a90a696b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydrochlorothiazide

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075640

Marketing category

ANDA

Marketing start

2017-08-10

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

13 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record