Benicar HCT

Product NDC
55289-443
11-digit product format
552890443
Labeler code
55289
Product ID
55289-443_7c4889dd-2a20-f1ec-e053-2991aa0a0e0c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
olmesartan medoxomil-hydrochlorothiazide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-443-30EA - Each55289-4437de231cb-7c65-4c99-a7d1-32d184f897aa12012-07-24