Fosinopril sodium

Product NDC

50090-3444

11-digit product format

500903444

Labeler code

50090

Product ID

50090-3444_458f0c70-6453-4068-8a2c-95bfd8f4e411

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fosinopril sodium

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077222

Marketing category

ANDA

Marketing start

2005-06-21

Marketing end

0000-00-00

Substance

FOSINOPRIL SODIUM

Active strength

10 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