Losartan Potassium

Product NDC
50090-2622
11-digit product format
500902622
Labeler code
50090
Product ID
50090-2622_8ff646c2-1063-4813-a475-c4c42c2bd2f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090083
Marketing category
ANDA
Marketing start
2010-10-06
Substance
LOSARTAN POTASSIUM
Active strength
25 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 POTASSIUM25 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3ST302B24A
Rxcui979480, 979485, 979492

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2622-0Losartan Potassium30 in 1 BOTTLETABLET, FILM COATED3036
50090-2622-1Losartan Potassium90 in 1 BOTTLETABLET, FILM COATED9036
50090-2622-2Losartan Potassium100 in 1 BOTTLETABLET, FILM COATED10036

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2622LOSARTAN POTASSIUM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]34Current NDC, Legacy NDC, 3 package rows20240206_73bb1210-fa46-4c88-b07c-14ff5580ef18.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979480losartan potassium 100 MG Oral TabletPSN73bb1210-fa46-4c88-b07c-14ff5580ef1836
979485losartan potassium 25 MG Oral TabletPSN73bb1210-fa46-4c88-b07c-14ff5580ef1836
979492losartan potassium 50 MG Oral TabletPSN73bb1210-fa46-4c88-b07c-14ff5580ef1836
979480losartan potassium 100 MG Oral TabletSCD73bb1210-fa46-4c88-b07c-14ff5580ef1836
979485losartan potassium 25 MG Oral TabletSCD73bb1210-fa46-4c88-b07c-14ff5580ef1836
979492losartan potassium 50 MG Oral TabletSCD73bb1210-fa46-4c88-b07c-14ff5580ef1836
979480Losartan K+ 100 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836
979485Losartan K+ 25 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836
979492Losartan K+ 50 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836
979480Losartan Pot 100 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836
979485Losartan Pot 25 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836
979492Losartan Pot 50 MG Oral TabletSY73bb1210-fa46-4c88-b07c-14ff5580ef1836

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-2622-05009026220030 TABLET, FILM COATED in 1 BOTTLE (50090-2622-0) 2016-12-070000-00-00NoNoCurrent
50090-2622-15009026220190 TABLET, FILM COATED in 1 BOTTLE (50090-2622-1) 2016-11-160000-00-00NoNoCurrent
50090-2622-250090262202100 TABLET, FILM COATED in 1 BOTTLE (50090-2622-2) 2023-10-26NoNoCurrent