Benicar HCT

Product NDC

50090-1083

11-digit product format

500901083

Labeler code

50090

Product ID

50090-1083_6e114be5-3209-4dfa-88c3-05ed7d6b37e3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

olmesartan medoxomil-hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA021532

Marketing category

NDA

Marketing start

2003-06-05

Marketing end

0000-00-00

Substance

OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE

Active strength

40 mg/1; mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record