Fosinopril Sodium and Hydrochlorothiazide

Product NDC

23155-061

11-digit product format

231550061

Labeler code

23155

Product ID

23155-061_ae9c745c-8bf7-4d50-81a9-afb4a9ee3aa7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fosinopril Sodium and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Application

ANDA079025

Marketing category

ANDA

Marketing start

2011-11-15

Marketing end

0000-00-00

Substance

FOSINOPRIL SODIUM; 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

2020-12-31

Current FDA listing

Historical FDA.report record