OLMESARTAN MEDOXOMIL
These highlights do not include all the information needed to use OLMESARTAN MEDOXOMIL TABLETS safely and effectively. See full prescribing information for OLMESARTAN MEDOXOMIL TABLETS. OLMESARTAN MEDOXOMIL tablets, for oral useInitial U.S. Approval: 2002
Approved
Approval ID
05a807bf-5175-43a2-a676-215bba2645a8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 15, 2023
Manufacturers
FDA
Inventia Healthcare Limited
DUNS: 650452522
Products 3
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
OLMESARTAN MEDOXOMIL
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49252-067
Application NumberANDA208659
Product Classification
M
Marketing Category
C73584
G
Generic Name
OLMESARTAN MEDOXOMIL
Product Specifications
Route of AdministrationORAL
Effective DateDecember 21, 2022
FDA Product Classification
INGREDIENTS (9)
OLMESARTAN MEDOXOMILActive
Quantity: 40 mg in 1 1
Code: 6M97XTV3HD
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTEDInactive
Code: 2165RE0K14
Classification: IACT
HYPROMELLOSE 2910 (15 MPA.S)Inactive
Code: 36SFW2JZ0W
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive
Code: RFW2ET671P
Classification: IACT
olmesartan medoxomil
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49252-066
Application NumberANDA208659
Product Classification
M
Marketing Category
C73584
G
Generic Name
olmesartan medoxomil
Product Specifications
Route of AdministrationORAL
Effective DateDecember 21, 2022
FDA Product Classification
INGREDIENTS (9)
OLMESARTAN MEDOXOMILActive
Quantity: 20 mg in 1 1
Code: 6M97XTV3HD
Classification: ACTIB
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTEDInactive
Code: 2165RE0K14
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
HYPROMELLOSE 2910 (15 MPA.S)Inactive
Code: 36SFW2JZ0W
Classification: IACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive
Code: RFW2ET671P
Classification: IACT
olmesartan medoxomil
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49252-065
Application NumberANDA208659
Product Classification
M
Marketing Category
C73584
G
Generic Name
olmesartan medoxomil
Product Specifications
Route of AdministrationORAL
Effective DateDecember 21, 2022
FDA Product Classification
INGREDIENTS (10)
OLMESARTAN MEDOXOMILActive
Quantity: 5 mg in 1 1
Code: 6M97XTV3HD
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTEDInactive
Code: 2165RE0K14
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
HYPROMELLOSE 2910 (15 MPA.S)Inactive
Code: 36SFW2JZ0W
Classification: IACT
FERRIC OXIDE YELLOWInactive
Code: EX438O2MRT
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive
Code: RFW2ET671P
Classification: IACT