lisinopril

Product NDC
68001-270
11-digit product format
680010270
Labeler code
68001
Product ID
68001-270_9494cf39-52ea-496c-89ac-5915bb2f0d8b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
BluePoint Laboratories
Application
ANDA075994
Marketing category
ANDA
Marketing start
2015-07-06
Marketing end
2020-04-30
Substance
LISINOPRIL
Active strength
30 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
68001-270-00EA - Each68001-270140b18dd-ae88-4f35-aad6-51ed91f1dde112015-08-04