Fosinopril Sodium

Product NDC

67544-322

11-digit product format

675440322

Labeler code

67544

Product ID

67544-322_1e4cd5c0-6b72-4fae-a4c7-95f8ef34cc87

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fosinopril Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Aphena Pharma Solutions - Tennessee, Inc.

Application

ANDA076483

Marketing category

ANDA

Marketing start

2004-04-23

Marketing end

0000-00-00

Substance

FOSINOPRIL SODIUM

Active strength

20 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record