olmesartan medoxomil and hydrochlorothiazide (70518-2269)

Drug Facts

Product Profile

Brand Name olmesartan medoxomil and hydrochlorothiazide

Generic Name olmesartan medoxomil and hydrochlorothiazide

Labeler remedyrepack inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, olmesartan medoxomil 40 mg/1

Manufacturer

REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2269

Product ID 70518-2269_49f0288b-29b6-d4b6-e063-6394a90a22ad

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA204233

Listing Expiration 2027-12-31

Marketing Start 2019-08-16

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 705182269

Hyphenated Format 70518-2269

Supplemental Identifiers

RxCUI

403854

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 ANDA204233 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
40 mg/1

source: ndc

Packaging

90 TABLET in 1 BOTTLE, PLASTIC (70518-2269-0)

source: ndc

Packages (1)

70518-2269-0 90 TABLET in 1 BOTTLE, PLASTIC (70518-2269-0)

Ingredients (2)

hydrochlorothiazide (12.5 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": "49f0288b-29b6-d4b6-e063-6394a90a22ad", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403854"], "spl_set_id": ["de815d64-b8d4-46a8-95b8-c230abe7f767"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2269-0)", "package_ndc": "70518-2269-0", "marketing_start_date": "20190816"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "70518-2269_49f0288b-29b6-d4b6-e063-6394a90a22ad", "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": "70518-2269", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "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": "40 mg/1"}], "application_number": "ANDA204233", "marketing_category": "ANDA", "marketing_start_date": "20190816", "listing_expiration_date": "20271231"}