Fosinopril Sodium

Product NDC

50090-1112

11-digit product format

500901112

Labeler code

50090

Product ID

50090-1112_d68a494d-99fe-4c46-aba7-5abe6b1f2ec2

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

2007-09-17

Marketing end

0000-00-00

Substance

FOSINOPRIL SODIUM

Active strength

40 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