Olmesartan Medoxomil

Product NDC
71335-2600
11-digit product format
713352600
Labeler code
71335
Product ID
71335-2600_c9a7aa4e-1d94-4f7e-a368-316d794083c4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Olmesartan Medoxomil
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA206763
Marketing category
ANDA
Marketing start
2017-04-24
Substance
OLMESARTAN MEDOXOMIL
Active strength
5 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

openFDA Listing Details

Product ID
71335-2600_c9a7aa4e-1d94-4f7e-a368-316d794083c4
Product type
HUMAN PRESCRIPTION DRUG
Finished product
Yes
Brand name base
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Dosage form
TABLET, COATED
Route
ORAL
Marketing start
2017-04-24
Marketing category
ANDA
Application number
ANDA206763
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]
Listing expiration
2026-12-31

Related Records

openFDA Active Ingredients

IngredientStrength
OLMESARTAN MEDOXOMIL5 mg/1

openFDA Harmonized Identifiers

FieldValues
Unii6M97XTV3HD
Rxcui349373
Spl Set Ideff499eb-a0e4-4240-870c-83bb53434cc2
Manufacturer NameBryant Ranch Prepack

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
6M97XTV3HDOLMESARTAN MEDOXOMIL144689-63-4OLMESARTAN MEDOXOMIL

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2600-17133526000190 TABLET, COATED in 1 BOTTLE (71335-2600-1) 2025-06-05NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Olmesartan MedoxomilBryant Ranch Prepack2025-10-24HUMAN PRESCRIPTION DRUG LABEL2