Lisinopril

Product NDC
68788-8351
11-digit product format
687888351
Labeler code
68788
Product ID
68788-8351_85b2cd38-732d-4047-ac69-5374f28a7cd2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA077321
Marketing category
ANDA
Marketing start
2023-02-07
Substance
LISINOPRIL
Active strength
20 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-8351-1EA - Each68788-8351b53a5dca-eb8b-4796-81a7-dbc8176853ac12023-03-13
68788-8351-3EA - Each68788-8351de659e5e-f8f8-4822-a8c8-ee1fc1bb028712023-03-13
68788-8351-6EA - Each68788-8351eeda441b-85c6-4cbb-8030-227610f0ac4312023-03-13
68788-8351-9EA - Each68788-8351d5161fa5-8fe3-4406-86ac-8c7503718a6612023-03-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-8351LISINOPRIL TABLET [PREFERRED PHARMACEUTICALS, INC.]2Current NDC20250117_b53aee22-52c7-47b1-95fc-e5383b5e6f58.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68788-8351-168788835101100 TABLET in 1 BOTTLE (68788-8351-1) 100 tablet2023-02-07NoNoHistorical
68788-8351-36878883510330 TABLET in 1 BOTTLE (68788-8351-3) 30 tablet2023-02-07NoNoHistorical
68788-8351-66878883510660 TABLET in 1 BOTTLE (68788-8351-6) 60 tablet2023-02-07NoNoHistorical
68788-8351-96878883510990 TABLET in 1 BOTTLE (68788-8351-9) 90 tablet2023-02-07NoNoHistorical