Fosinopril sodium

Product NDC
50090-3428
11-digit product format
500903428
Labeler code
50090
Product ID
50090-3428_c012fe48-c5e9-4334-a16f-9b4a141217d8
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
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3428-0EA - Each50090-3428c904862f-31a0-4923-95f1-9e87a851ec8c12019-05-02