Valsartan

Product NDC
71335-2248
11-digit product format
713352248
Labeler code
71335
Product ID
71335-2248_2a567e86-d264-4b4d-89e9-19aa65d2c2df
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
valsartan
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA204821
Marketing category
ANDA
Marketing start
2015-08-31
Substance
VALSARTAN
Active strength
160 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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
80M03YXJ7IVALSARTAN137862-53-4VALSARTAN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2248-17133522480130 TABLET in 1 BOTTLE (71335-2248-1) 30 tablet2023-09-25NoNoHistorical
71335-2248-27133522480290 TABLET in 1 BOTTLE (71335-2248-2) 90 tablet2023-09-25NoNoHistorical
71335-2248-371335224803120 TABLET in 1 BOTTLE (71335-2248-3) 120 tablet2023-09-25NoNoHistorical
71335-2248-471335224804180 TABLET in 1 BOTTLE (71335-2248-4) 180 tablet2023-09-25NoNoHistorical
71335-2248-57133522480528 TABLET in 1 BOTTLE (71335-2248-5) 28 tablet2023-09-25NoNoHistorical
71335-2248-67133522480660 TABLET in 1 BOTTLE (71335-2248-6) 60 tablet2023-09-25NoNoHistorical
71335-2248-771335224807100 TABLET in 1 BOTTLE (71335-2248-7) 100 tablet2023-09-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ValsartanBryant Ranch Prepack2023-09-25HUMAN PRESCRIPTION DRUG LABEL100