Fosinopril Sodium

Product NDC
67544-306
11-digit product format
675440306
Labeler code
67544
Product ID
67544-306_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
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
67544-306-30EA - Each67544-3066fc8922f-eb18-40be-8690-3c52fd61818c12013-02-13
67544-306-45EA - Each67544-30637aff17c-96d0-489b-892d-83f2157c971012013-02-13
67544-306-60EA - Each67544-306645698c8-b142-4341-9b2c-b715feafca4312013-02-13