Lisinopril

Product NDC
63629-2688
11-digit product format
636292688
Labeler code
63629
Product ID
63629-2688_64edab84-7e69-48c4-8cce-b3588fb441f9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076059
Marketing category
ANDA
Marketing start
2002-07-01
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
10 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
E7199S1YWRLISINOPRIL83915-83-7LISINOPRIL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-2688-16362926880130 TABLET in 1 BOTTLE (63629-2688-1) 30 tablet2011-04-150000-00-00NoNoCurrent
63629-2688-263629268802100 TABLET in 1 BOTTLE (63629-2688-2) 100 tablet2011-04-150000-00-00NoNoCurrent
63629-2688-36362926880360 TABLET in 1 BOTTLE (63629-2688-3) 60 tablet2011-04-150000-00-00NoNoCurrent
63629-2688-46362926880490 TABLET in 1 BOTTLE (63629-2688-4) 90 tablet2011-04-150000-00-00NoNoCurrent
63629-2688-56362926880520 TABLET in 1 BOTTLE (63629-2688-5) 20 tablet2011-04-150000-00-00NoNoCurrent
63629-2688-663629268806120 TABLET in 1 BOTTLE (63629-2688-6) 120 tablet2005-05-100000-00-00NoNoCurrent
63629-2688-7636292688077 TABLET in 1 BOTTLE (63629-2688-7) 7 tablet2005-05-100000-00-00NoNoCurrent
63629-2688-86362926880815 TABLET in 1 BOTTLE (63629-2688-8) 15 tablet2011-04-150000-00-00NoNoCurrent