LOSARTAN POTASSIUM

Product NDC
71335-1136
11-digit product format
713351136
Labeler code
71335
Product ID
71335-1136_844e9245-1cfa-400c-b2d5-93a5924290a8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091541
Marketing category
ANDA
Marketing start
2012-12-06
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

Related Records

Active Ingredients

IngredientStrength
LOSARTAN POTASSIUM25 mg/1

Harmonized Identifiers

FieldValues
Unii3ST302B24A
Rxcui979485

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
3ST302B24ALOSARTAN POTASSIUM124750-99-8LOSARTAN POTASSIUM

Packages

Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1136-17133511360190 TABLET, FILM COATED in 1 BOTTLE (71335-1136-1) 2022-02-140000-00-00NoNoCurrent
71335-1136-27133511360230 TABLET, FILM COATED in 1 BOTTLE (71335-1136-2) 2019-03-210000-00-00NoNoCurrent
71335-1136-37133511360360 TABLET, FILM COATED in 1 BOTTLE (71335-1136-3) 2019-03-040000-00-00NoNoCurrent
71335-1136-471335113604100 TABLET, FILM COATED in 1 BOTTLE (71335-1136-4) 2022-02-140000-00-00NoNoCurrent
71335-1136-57133511360510 TABLET, FILM COATED in 1 BOTTLE (71335-1136-5) 2022-02-140000-00-00NoNoCurrent
71335-1136-6713351136067 TABLET, FILM COATED in 1 BOTTLE (71335-1136-6) 2022-02-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LOSARTAN POTASSIUMBryant Ranch Prepack2025-09-18HUMAN PRESCRIPTION DRUG LABEL3