lisinopril

Product NDC
68001-272
11-digit product format
680010272
Labeler code
68001
Product ID
68001-272_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
2016-09-07
Marketing end
2019-08-31
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
68001-272-00EA - Each68001-272fac6fa0c-80aa-4b4e-a632-85e6fa594b3c12017-03-06
68001-272-08EA - Each68001-27249c5b24f-74bd-4332-9eff-4de7cf5c5aea12017-03-06