Lisinopril and Hydrochlorothiazide

Product NDC

50090-2634

11-digit product format

500902634

Labeler code

50090

Product ID

50090-2634_0b73a7bf-2fc4-4354-998c-e847ec3eb7ec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA076262

Marketing category

ANDA

Marketing start

2002-07-02

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record