valsartan and hydrochlorothiazide (65862-551)

Drug Facts

Product Profile

Brand Name valsartan and hydrochlorothiazide

Generic Name valsartan and hydrochlorothiazide

Labeler aurobindo pharma limited

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, valsartan 320 mg/1

Manufacturer

Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-551

Product ID 65862-551_81a03db7-4be2-478d-b625-e59c8bd2235f

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA202519

Listing Expiration 2026-12-31

Marketing Start 2013-03-21

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc] angiotensin 2 receptor blocker [epc]

Mechanism of Action

angiotensin 2 receptor antagonists [moa]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862551

Hyphenated Format 65862-551

Supplemental Identifiers

RxCUI

200284 200285 349353 636042 636045

UNII

0J48LPH2TH 80M03YXJ7I

NUI

N0000175359 N0000175419 M0471776 N0000000070 N0000175561

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 valsartan and hydrochlorothiazide (source: ndc)

Generic Name valsartan and hydrochlorothiazide (source: ndc)

Application Number ANDA202519 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
320 mg/1

source: ndc

Packaging

500 TABLET, FILM COATED in 1 BOTTLE (65862-551-05)
90 TABLET, FILM COATED in 1 BOTTLE (65862-551-90)

source: ndc

Packages (2)

65862-551-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-551-05) 65862-551-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-551-90)

Ingredients (2)

hydrochlorothiazide (25 mg/1) valsartan (320 mg/1)

Linked Drug Pages (1)

Valsartan and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "81a03db7-4be2-478d-b625-e59c8bd2235f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["c5bc7c55-b50c-4e61-ad1f-5ebb607c262f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-551-05)", "package_ndc": "65862-551-05", "marketing_start_date": "20130321"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-551-90)", "package_ndc": "65862-551-90", "marketing_start_date": "20130321"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "65862-551_81a03db7-4be2-478d-b625-e59c8bd2235f", "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": "65862-551", "generic_name": "Valsartan and Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA202519", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}