olmesartan medoxomil

Product NDC
71335-2380
11-digit product format
713352380
Labeler code
71335
Product ID
71335-2380_5bb43e02-654a-4321-b01f-eb4b3fd7e8f7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
olmesartan medoxomil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208130
Marketing category
ANDA
Marketing start
2018-06-29
Substance
OLMESARTAN MEDOXOMIL
Active strength
40 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
6M97XTV3HDOLMESARTAN MEDOXOMIL144689-63-4OLMESARTAN MEDOXOMIL

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2380-17133523800130 TABLET, FILM COATED in 1 BOTTLE (71335-2380-1) 2024-05-29NoNoHistorical
71335-2380-27133523800290 TABLET, FILM COATED in 1 BOTTLE (71335-2380-2) 2024-05-29NoNoHistorical
71335-2380-37133523800328 TABLET, FILM COATED in 1 BOTTLE (71335-2380-3) 2024-05-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
olmesartan medoxomilBryant Ranch Prepack2024-05-29HUMAN PRESCRIPTION DRUG LABEL1