olmesartan medoxomil and hydrochlorothiazide

Generic: olmesartan medoxomil and hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil and hydrochlorothiazide
Generic Name olmesartan medoxomil and hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1, olmesartan medoxomil 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2424
Product ID 71335-2424_512a8b29-e8bb-4ebb-a799-98b2caab806c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207804
Listing Expiration 2026-12-31
Marketing Start 2017-04-24

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352424
Hyphenated Format 71335-2424

Supplemental Identifiers

RxCUI
403853
UNII
0J48LPH2TH 6M97XTV3HD
NUI
N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name olmesartan medoxomil and hydrochlorothiazide (source: ndc)
Generic Name olmesartan medoxomil and hydrochlorothiazide (source: ndc)
Application Number ANDA207804 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2424-1)
  • 60 TABLET in 1 BOTTLE (71335-2424-2)
  • 90 TABLET in 1 BOTTLE (71335-2424-3)
source: ndc

Packages (3)

71335-2424-1 30 TABLET in 1 BOTTLE (71335-2424-1) 71335-2424-2 60 TABLET in 1 BOTTLE (71335-2424-2) 71335-2424-3 90 TABLET in 1 BOTTLE (71335-2424-3)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) olmesartan medoxomil (20 mg/1)

Linked Drug Pages (1)

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "512a8b29-e8bb-4ebb-a799-98b2caab806c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853"], "spl_set_id": ["68d44330-4213-46a7-97b9-f858c16454d1"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2424-1)", "package_ndc": "71335-2424-1", "marketing_start_date": "20240701"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2424-2)", "package_ndc": "71335-2424-2", "marketing_start_date": "20240701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2424-3)", "package_ndc": "71335-2424-3", "marketing_start_date": "20240701"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "71335-2424_512a8b29-e8bb-4ebb-a799-98b2caab806c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-2424", "generic_name": "olmesartan medoxomil and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207804", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}