Lisinopril

Product NDC
0378-2072
11-digit product format
003782072
Labeler code
0378
Product ID
0378-2072_f7c37d53-b108-4794-8e07-c7726a12b8c0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA076071
Marketing category
ANDA
Marketing start
2002-07-01
Marketing end
2019-06-30
Substance
LISINOPRIL
Active strength
3 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-2072-01EA - Each0378-20723f84e501-d3f4-4cd1-ace0-b42f840840ab12012-07-24