Lisinopril

Product NDC
68788-8310
11-digit product format
687888310
Labeler code
68788
Product ID
68788-8310_73d1f211-5977-41cb-88c8-65aaf9141374
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA077321
Marketing category
ANDA
Marketing start
2022-12-20
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
2026-12-31
Current FDA listing
Yes

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-8310-1EA - Each68788-83105c5d9b56-425a-4699-b8a2-bbb661e12e3e12023-02-06
68788-8310-3EA - Each68788-8310cd088638-cc3b-4a0b-91e9-d1c550cd09e112023-02-06
68788-8310-6EA - Each68788-8310c402694f-2cfb-4c8a-874e-20a75cad190f12023-02-06
68788-8310-9EA - Each68788-83107de7adb8-701d-4cd5-92b0-050c95d795c412023-02-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-8310LISINOPRIL TABLET [PREFERRED PHARMACEUTICALS, INC.]3Current NDC, Legacy NDC20240625_35133fb0-9026-4dbc-9325-b64569696467.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-8310-168788831001100 TABLET in 1 BOTTLE (68788-8310-1) 100 tablet2022-12-200000-00-00NoNoCurrent
68788-8310-36878883100330 TABLET in 1 BOTTLE (68788-8310-3) 30 tablet2022-12-200000-00-00NoNoCurrent
68788-8310-66878883100660 TABLET in 1 BOTTLE (68788-8310-6) 60 tablet2022-12-200000-00-00NoNoCurrent
68788-8310-96878883100990 TABLET in 1 BOTTLE (68788-8310-9) 90 tablet2022-12-200000-00-00NoNoCurrent