FDA.reportPublic FDA data

Losartan Potassium

Product NDC
71335-1235
11-digit product format
713351235
Labeler code
71335
Product ID
71335-1235_2e19e89b-daac-449a-a511-217ed561f5fd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090083
Marketing category
ANDA
Marketing start
2010-10-06
Substance
LOSARTAN POTASSIUM
Active strength
100 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 POTASSIUM100 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3ST302B24A
Rxcui979480

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
71335-1235-1Losartan Potassium30 in 1 BOTTLETABLET, FILM COATED30104
71335-1235-2Losartan Potassium60 in 1 BOTTLETABLET, FILM COATED60104
71335-1235-3Losartan Potassium90 in 1 BOTTLETABLET, FILM COATED90104
71335-1235-4Losartan Potassium120 in 1 BOTTLETABLET, FILM COATED120104
71335-1235-5Losartan Potassium100 in 1 BOTTLETABLET, FILM COATED100104
71335-1235-6Losartan Potassium28 in 1 BOTTLETABLET, FILM COATED28104
71335-1235-7Losartan Potassium10 in 1 BOTTLETABLET, FILM COATED10104
71335-1235-8Losartan Potassium180 in 1 BOTTLETABLET, FILM COATED180104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1235LOSARTAN POTASSIUM TABLET, FILM COATED [BRYANT RANCH PREPACK]103Current NDC, Legacy NDC, 8 package rows20240724_4d7a0e82-4791-4e3f-932a-2f1a2993ba36.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979480losartan potassium 100 MG Oral TabletPSN4d7a0e82-4791-4e3f-932a-2f1a2993ba36104
979480losartan potassium 100 MG Oral TabletSCD4d7a0e82-4791-4e3f-932a-2f1a2993ba36104
979480Losartan K+ 100 MG Oral TabletSY4d7a0e82-4791-4e3f-932a-2f1a2993ba36104
979480Losartan Pot 100 MG Oral TabletSY4d7a0e82-4791-4e3f-932a-2f1a2993ba36104

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1235-17133512350130 TABLET, FILM COATED in 1 BOTTLE (71335-1235-1) 2019-05-300000-00-00NoNoCurrent
71335-1235-27133512350260 TABLET, FILM COATED in 1 BOTTLE (71335-1235-2) 2024-07-090000-00-00NoNoCurrent
71335-1235-37133512350390 TABLET, FILM COATED in 1 BOTTLE (71335-1235-3) 2019-06-210000-00-00NoNoCurrent
71335-1235-471335123504120 TABLET, FILM COATED in 1 BOTTLE (71335-1235-4) 2024-07-090000-00-00NoNoCurrent
71335-1235-571335123505100 TABLET, FILM COATED in 1 BOTTLE (71335-1235-5) 2024-07-090000-00-00NoNoCurrent
71335-1235-67133512350628 TABLET, FILM COATED in 1 BOTTLE (71335-1235-6) 2024-07-090000-00-00NoNoCurrent
71335-1235-77133512350710 TABLET, FILM COATED in 1 BOTTLE (71335-1235-7) 2019-09-030000-00-00NoNoCurrent
71335-1235-871335123508180 TABLET, FILM COATED in 1 BOTTLE (71335-1235-8) 2024-07-090000-00-00NoNoCurrent