FDA.reportPublic FDA data

LISINOPRIL

Product NDC
35356-948
11-digit product format
353560948
Labeler code
35356
Product ID
35356-948_90f89a42-ac1e-4a5d-a351-19f073dc92a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LISINOPRIL
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA077321
Marketing category
ANDA
Marketing start
2007-02-15
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
40 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-948-30EA - Each35356-94828f73b41-cfd2-4e81-8100-63033a33dab112013-09-04
35356-948-60EA - Each35356-948c4231a82-2791-46f6-8f37-7ff7ff32e2e012013-09-04
35356-948-90EA - Each35356-9481a379d72-9b36-4029-a3b5-a9b12d22066f12013-09-04