FDA.reportPublic FDA data

NDC 65862-603-10 - Moxifloxacin Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
65862-603
Requested NDC
65862-603-10
Package NDCs from labels
65862-603-30, 65862-603-99, 65862-603-10, 65862-603-55
Manufacturer
American Health Packaging
Effective date
2026-07-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Moxifloxacin Hydrochloride - American Health PackagingAmerican Health Packaging2026-07-02HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - REMEDYREPACK INC.REMEDYREPACK INC.2026-05-18HUMAN PRESCRIPTION DRUG LABEL
Moxifloxacin Hydrochloride - AvPAKAvPAK2026-04-07HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - PD-Rx Pharmaceuticals, Inc.PD-Rx Pharmaceuticals, Inc.2026-02-16HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - PD-Rx Pharmaceuticals, Inc.PD-Rx Pharmaceuticals, Inc.2026-02-16HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - Bryant Ranch PrepackBryant Ranch Prepack2026-02-02HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - Major PharmaceuticalsMajor Pharmaceuticals2025-12-17HUMAN PRESCRIPTION DRUG LABEL
MOXIFLOXACIN HYDROCHLORIDE - Aurobindo Pharma LimitedAurobindo Pharma Limited2025-09-01Human Prescription Drug Label
MOXIFLOXACIN HYDROCHLORIDE - A-S Medication SolutionsA-S Medication Solutions2024-09-18Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65862-603-10MOXIFLOXACIN HYDROCHLORIDE1 in 1 BLISTER PACKTABLET, FILM COATED117
65862-603-30MOXIFLOXACIN HYDROCHLORIDE30 in 1 BOTTLETABLET, FILM COATED3017
65862-603-55MOXIFLOXACIN HYDROCHLORIDE50 in 1 BOX, UNIT-DOSETABLET, FILM COATED5017
65862-603-99MOXIFLOXACIN HYDROCHLORIDE1000 in 1 BOTTLETABLET, FILM COATED100017

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65862-603MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]16Current NDC, Legacy NDC, 4 package rows20241213_d6789c17-4a2f-4519-9060-e3b0dba422f0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-603-30EA - Each65862-6033ea07df5-d4cb-42b0-96e6-d47f01ba070512014-04-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MOXIFLOXACIN HYDROCHLORIDEACTIVE INGREDIENTC53598599TMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
MOXIFLOXACINACTIVE MOIETYU188XYD42PMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
HYPROMELLOSE 2910 (6 MPA.S)INACTIVE INGREDIENT0WZ8WG20P6MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
POLYETHYLENE GLYCOL 4000INACTIVE INGREDIENT4R4HFI6D95MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
POVIDONE K30INACTIVE INGREDIENTU725QWY32XMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]2
MOXIFLOXACIN HYDROCHLORIDEACTIVE INGREDIENTC53598599TMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
MOXIFLOXACINACTIVE MOIETYU188XYD42PMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
HYPROMELLOSE 2910 (6 MPA.S)INACTIVE INGREDIENT0WZ8WG20P6MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
POLYETHYLENE GLYCOL 4000INACTIVE INGREDIENT4R4HFI6D95MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
POVIDONE K30INACTIVE INGREDIENTU725QWY32XMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPMOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 106 · 2,112 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CalamineFERRIC OXIDE REDThe Kroger Co.9ddcd6ba-1aed-48f8-a91a-54bd6f0d93082026-08-06Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
EltaMD UV RestoreTITANIUM DIOXIDE, ZINC OXIDE SUNSCREENCP Skin Health Group, Inc37fee381-ce6b-4949-9a4a-778aa839fb842026-08-06WarningsExact identifier
unii: 15FIX9V2JP
MOXIFLOXACINMOXIFLOXACINA-S Medication Solutionsf702e112-b037-4e50-ac30-b1d27fc0e30e2026-08-05Warnings, Adverse reactionsExact identifier
unii: C53598599T
Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEYOCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8%Lale Cosmetics LLC581fb0cd-c55d-d562-e063-6394a90a7f112026-08-03WarningsExact identifier
unii: 15FIX9V2JP
EltaMD UV ActiveZINC OXIDE AND TITANIUM DIOXIDE SUNSCREENCP Skin Health Group, Inc39d16479-d491-4c19-aa11-674461687c7b2026-08-03WarningsExact identifier
unii: 15FIX9V2JP
Continuous Correction CreamTITANIUM DIOXIDEBaxter of California, LLC1cbcc648-f2e1-af60-e063-6294a90ad4bb2026-07-31WarningsExact identifier
unii: 15FIX9V2JP
Cover CremeTITANIUM DIOXIDEBaxter of California31f5e8c4-523f-4596-e063-6294a90a6a122026-07-31WarningsExact identifier
unii: 15FIX9V2JP
ESIKA COLORFIX POLVOS 32H POLVO COMPACTO FACIAL DE ALTA COBERTURA FPS 15 110-COCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDEBEL STAR S.A.575fb2c3-e332-8a3b-e063-6394a90a9fd92026-07-24WarningsExact identifier
unii: 15FIX9V2JP
True Coast SPF 50 Mineral SunscreenZINC OXIDE 18%, TITANIUM DIOXIDE 6%Foshan Sugar Max Cosmetics CO.,Ltd5379466d-8d14-5fc2-e063-6394a90abd7e2026-07-22WarningsExact identifier
unii: 15FIX9V2JP
CalamineCALAMINE AND ZINC OXIDEMarie's Original Formulas LLC57110309-9a3d-025f-e063-6394a90a015a2026-07-22WarningsExact identifier
unii: 1K09F3G675
Yves Saint Laurent All Hours Foundation Sunscreen Broad Spectrum SPF 30 Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDESICOS ET CIE571f23e9-1126-e32d-e063-6294a90a99512026-07-21WarningsExact identifier
unii: 15FIX9V2JP
MENS SPF50 ALL IN ONE SUNSCREENMENS SPF50 ALL IN ONE SUNSCREENLance (Guangzhou) Biological Technology Co., Ltd.57074480-77fd-cc06-e063-6294a90a28d42026-07-20WarningsExact identifier
unii: 15FIX9V2JP
CalamineCALAMINE AND ZINC OXIDEMarie's Original Formulas LLC571083ce-cd35-a638-e063-6394a90ae4c72026-07-20WarningsExact identifier
unii: 1K09F3G675
Yves Saint Laurent All Hours Foundation Sunscreen Broad Spectrum SPF 30 Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Inc5711364c-f9b4-bfa6-e063-6294a90ace4a2026-07-20WarningsExact identifier
unii: 15FIX9V2JP
CalamineFERRIC OXIDE REDBetter Living Brands, LLCc7ef0ef3-6861-4b94-af4b-371fee8c1f3d2026-07-16Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
Bombee Honey Daily Glow Shield SunscreenHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEABT ASIA Inc.56112dff-b091-7a56-e063-6294a90a77d32026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DERMIO DERMATOLOGY LLC562f5b0d-6a10-305d-e063-6394a90a59802026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30Suzanne's Skin2soul LLC562fbaa6-f93a-5ec4-e063-6294a90a96342026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Aussie Betta Tallow Sunscreen SPF50 SPF50TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREENAUSSIE BETTA HEALTHY CARE PTY LTD56007d82-ff5b-6c26-e063-6294a90a09b62026-07-07WarningsExact identifier
unii: 15FIX9V2JP
EELHOE Body Coverage PerfectorTITANIUM DIOXIDEShantou Eelhoe Daily Chemical Technology Co., Ltd.5610c3b7-456b-3bc1-e063-6394a90a3fa82026-07-07WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.