Lisinopril and Hydrochlorothiazide

Product NDC

57237-243

11-digit product format

572370243

Labeler code

57237

Product ID

57237-243_e401ab79-73cc-49fc-8aec-2c7aecb95b34

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Citron Pharma LLC

Application

ANDA077606

Marketing category

ANDA

Marketing start

2006-03-14

Marketing end

0000-00-00

Substance

LISINOPRIL; HYDROCHLOROTHIAZIDE

Active strength

20 mg/1; mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record