Losartan Potassium

Product NDC
68788-8189
11-digit product format
687888189
Labeler code
68788
Product ID
68788-8189_061d0838-f325-4fdb-8eb5-c0684f0df7db
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA091497
Marketing category
ANDA
Marketing start
2022-05-13
Substance
LOSARTAN POTASSIUM
Active strength
50 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Losartan Potassium
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LOSARTAN POTASSIUM50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3ST302B24A
Rxcui979492

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0d341e63-aee5-498b-bf9a-b53a43963acfProduct name120260105
de29c5c0-90ba-29da-d7ab-0500274708beProduct name620241009
15b375b1-89c7-9594-80df-5a8c8864aee0Product name320180108

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68788-8189-1Losartan Potassium100 in 1 BOTTLETABLET, FILM COATED1004
68788-8189-3Losartan Potassium30 in 1 BOTTLETABLET, FILM COATED304
68788-8189-6Losartan Potassium60 in 1 BOTTLETABLET, FILM COATED604
68788-8189-9Losartan Potassium90 in 1 BOTTLETABLET, FILM COATED904

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-8189-1EA - Each68788-818981d32555-5378-4402-88b3-f81881477fd812022-07-06
68788-8189-3EA - Each68788-81897b2188dc-a1f8-4724-a47e-f2d499c8b54a12022-07-06
68788-8189-6EA - Each68788-8189761d7e9a-b453-4c43-b1e7-fe0efc5095ea12022-07-06
68788-8189-9EA - Each68788-818922d917d0-0cc6-41cd-9d44-461a06feec2c12022-07-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-8189LOSARTAN POTASSIUM TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.]3Current NDC, Legacy NDC, 4 package rows20240628_68ed9727-987e-4bb6-98b4-b98150bb6404.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979492losartan potassium 50 MG Oral TabletPSN68ed9727-987e-4bb6-98b4-b98150bb64044
979492losartan potassium 50 MG Oral TabletSCD68ed9727-987e-4bb6-98b4-b98150bb64044
979492Losartan K+ 50 MG Oral TabletSY68ed9727-987e-4bb6-98b4-b98150bb64044
979492Losartan Pot 50 MG Oral TabletSY68ed9727-987e-4bb6-98b4-b98150bb64044

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-8189-168788818901100 TABLET, FILM COATED in 1 BOTTLE (68788-8189-1) 2022-05-130000-00-00NoNoCurrent
68788-8189-36878881890330 TABLET, FILM COATED in 1 BOTTLE (68788-8189-3) 2022-05-130000-00-00NoNoCurrent
68788-8189-66878881890660 TABLET, FILM COATED in 1 BOTTLE (68788-8189-6) 2022-05-130000-00-00NoNoCurrent
68788-8189-96878881890990 TABLET, FILM COATED in 1 BOTTLE (68788-8189-9) 2022-05-130000-00-00NoNoCurrent