olmesartan medoxomil and hydrochlorothiazide (71335-3031)

Drug Facts

Product Profile

Brand Name olmesartan medoxomil and hydrochlorothiazide

Generic Name olmesartan medoxomil and hydrochlorothiazide

Labeler bryant ranch prepack

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, olmesartan medoxomil 40 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-3031

Product ID 71335-3031_32704e35-a5c5-4a04-9a10-a4fc5ec8f188

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA204801

Listing Expiration 2027-12-31

Marketing Start 2023-06-02

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 713353031

Hyphenated Format 71335-3031

Supplemental Identifiers

RxCUI

403855

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 ANDA204801 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
40 mg/1

source: ndc

Packaging

90 TABLET, FILM COATED in 1 BOTTLE (71335-3031-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-3031-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-3031-3)

source: ndc

Packages (3)

71335-3031-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-3031-1) 71335-3031-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-3031-2) 71335-3031-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-3031-3)

Ingredients (2)

hydrochlorothiazide (25 mg/1) olmesartan medoxomil (40 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": "32704e35-a5c5-4a04-9a10-a4fc5ec8f188", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403855"], "spl_set_id": ["bb362b67-4a14-4491-9e12-0f7d5c7a65bc"], "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": "90 TABLET, FILM COATED in 1 BOTTLE (71335-3031-1)", "package_ndc": "71335-3031-1", "marketing_start_date": "20260205"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-3031-2)", "package_ndc": "71335-3031-2", "marketing_start_date": "20260205"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-3031-3)", "package_ndc": "71335-3031-3", "marketing_start_date": "20260205"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "71335-3031_32704e35-a5c5-4a04-9a10-a4fc5ec8f188", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-3031", "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": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA204801", "marketing_category": "ANDA", "marketing_start_date": "20230602", "listing_expiration_date": "20271231"}