FDA.reportPublic FDA data

Losartan Potassium

Product NDC
71335-0262
11-digit product format
713350262
Labeler code
71335
Product ID
71335-0262_570fae9a-6e7f-4704-8ca0-12aa2e12f3e0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091497
Marketing category
ANDA
Marketing start
2014-07-30
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
71335-0262-1Losartan Potassium30 in 1 BOTTLETABLET, FILM COATED307
71335-0262-2Losartan Potassium90 in 1 BOTTLETABLET, FILM COATED907
71335-0262-3Losartan Potassium60 in 1 BOTTLETABLET, FILM COATED607
71335-0262-4Losartan Potassium120 in 1 BOTTLETABLET, FILM COATED1207
71335-0262-5Losartan Potassium100 in 1 BOTTLETABLET, FILM COATED1007
71335-0262-6Losartan Potassium180 in 1 BOTTLETABLET, FILM COATED1807
71335-0262-7Losartan Potassium10 in 1 BOTTLETABLET, FILM COATED107

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0262-1EA - Each71335-02625517ab24-c642-4429-8963-8c2ccb3a2b4512018-03-08
71335-0262-2EA - Each71335-026284e812e9-56ff-4d2c-a809-84801221eceb12018-03-08
71335-0262-3EA - Each71335-026262ceab23-c3a7-48cd-8e0e-5414a951699812018-03-08
71335-0262-4EA - Each71335-0262c2e5562e-17f6-48ed-acf6-e5717983617812018-03-08
71335-0262-5EA - Each71335-02622c55848f-72e9-46fa-8e40-bb3bc87678a312018-03-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-0262LOSARTAN POTASSIUM TABLET, FILM COATED [BRYANT RANCH PREPACK]7Current NDC, Legacy NDC, 7 package rows20240829_43fa4762-cc0c-4a3b-a527-6aa7fb7c5464.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979492losartan potassium 50 MG Oral TabletPSN43fa4762-cc0c-4a3b-a527-6aa7fb7c54647
979492losartan potassium 50 MG Oral TabletSCD43fa4762-cc0c-4a3b-a527-6aa7fb7c54647
979492Losartan K+ 50 MG Oral TabletSY43fa4762-cc0c-4a3b-a527-6aa7fb7c54647
979492Losartan Pot 50 MG Oral TabletSY43fa4762-cc0c-4a3b-a527-6aa7fb7c54647

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0262-17133502620130 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1) 2019-04-220000-00-00NoNoCurrent
71335-0262-27133502620290 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2) 2019-04-030000-00-00NoNoCurrent
71335-0262-37133502620360 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3) 2022-01-200000-00-00NoNoCurrent
71335-0262-471335026204120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4) 2022-01-200000-00-00NoNoCurrent
71335-0262-571335026205100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5) 2022-01-200000-00-00NoNoCurrent
71335-0262-671335026206180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6) 2022-01-200000-00-00NoNoCurrent
71335-0262-77133502620710 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7) 2022-01-200000-00-00NoNoCurrent