olmesartan medoxomil and hydrochlorothiazide (31722-888)

Drug Facts

Product Profile

Brand Name olmesartan medoxomil and hydrochlorothiazide

Generic Name olmesartan medoxomil and hydrochlorothiazide

Labeler camber pharmaceuticals, inc.

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-888

Product ID 31722-888_3d401487-0f8f-9ee8-e063-6394a90ac68d

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209199

Listing Expiration 2026-12-31

Marketing Start 2025-07-25

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 31722888

Hyphenated Format 31722-888

Supplemental Identifiers

RxCUI

403853 403854 403855

UPC

0331722888301 0331722886307 0331722887304

UNII

0J48LPH2TH 6M97XTV3HD

NUI

N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager

true

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 ANDA209199 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
40 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (31722-888-30)
10 BLISTER PACK in 1 CARTON (31722-888-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90)

source: ndc

Packages (3)

31722-888-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-888-30) 31722-888-32 10 BLISTER PACK in 1 CARTON (31722-888-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK 31722-888-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90)

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": "3d401487-0f8f-9ee8-e063-6394a90ac68d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0331722888301", "0331722886307", "0331722887304"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["d421f352-9500-4d3e-8bc3-0cdcc2050514"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-888-30)", "package_ndc": "31722-888-30", "marketing_start_date": "20250725"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-888-32)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "31722-888-32", "marketing_start_date": "20250725"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90)", "package_ndc": "31722-888-90", "marketing_start_date": "20250725"}], "brand_name": "Olmesartan medoxomil and hydrochlorothiazide", "product_id": "31722-888_3d401487-0f8f-9ee8-e063-6394a90ac68d", "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": "31722-888", "generic_name": "Olmesartan medoxomil and hydrochlorothiazide", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "ANDA209199", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}