FDA.reportPublic FDA data

NDC 40032-022-30 - Linezolid

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
40032-022
Requested NDC
40032-022-30
Package NDCs from labels
40032-022-02, 40032-022-05, 40032-022-30, 40032-022-31
Manufacturer
Novel Laboratories, Inc.
Effective date
2019-12-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Linezolid - Novel Laboratories, Inc.Novel Laboratories, Inc.2019-12-21HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40032-022-022023-01-30C16284748780-1f386c64a-3db1-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use LINEZOLID TABLETS safely and effectively. See full prescribing information for LINEZOLID TABLETS. LINEZOLID tablets, for oral use Initial U.S. Approval:2000
40032-022-052023-01-30C16284748780-1f386c64a-3db1-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use LINEZOLID TABLETS safely and effectively. See full prescribing information for LINEZOLID TABLETS. LINEZOLID tablets, for oral use Initial U.S. Approval:2000
40032-022-312023-01-30C16284748780-1f386c64a-3db1-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use LINEZOLID TABLETS safely and effectively. See full prescribing information for LINEZOLID TABLETS. LINEZOLID tablets, for oral use Initial U.S. Approval:2000

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40032-022-02Linezolid20 in 1 BOTTLETABLET202
40032-022-05Linezolid500 in 1 BOTTLETABLET5002
40032-022-30Linezolid10 in 1 BLISTER PACKTABLET102
40032-022-31Linezolid3 in 1 CARTONTABLET32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40032-022LINEZOLID TABLET [NOVEL LABORATORIES, INC.]2Legacy NDC, 4 package rows20191222_13990ee8-8fbe-402d-8aba-cba78964fd32.zip

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 103 · 2,047 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
LinezolidLINEZOLIDSun Pharmaceutical Industries, Inc.870c9600-04d5-4b44-a5b5-02252a310f222026-07-31Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
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
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
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
LinezolidLINEZOLIDMacleods Pharmaceuticals Limited90dd8c13-c428-4472-91e5-5b1fcdc4fce32026-07-15Warnings, Adverse reactionsExact identifier
rxcui: 311347
unii: ISQ9I6J12J
LinezolidLINEZOLIDHikma Pharmaceuticals USA Inc.16007ca5-7956-4414-af38-406a6623400e2026-07-15Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
LinezolidLINEZOLIDEugia US LLCb721756c-3b5e-456d-a2f6-0d8a56cc7f352026-07-13Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
ZyvoxLINEZOLIDPharmacia & Upjohn Company LLC3e5e9975-6f36-42e4-ab46-0e75dda835922026-07-09Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
LinezolidLINEZOLIDMylan Pharmaceuticals Inc.83a84897-ccca-42a1-ab1a-bbf1d43a982b2026-07-09Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
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
Premier Tinted Mineral SunscreenBROAD SPECTRUM SPF30Emerald Aesthetics LLC55f88dd1-346c-22a5-e063-6294a90a711f2026-07-06WarningsExact identifier
unii: 15FIX9V2JP
LinezolidLINEZOLIDSportpharm LLC7368298b-d75c-4950-bbc1-00fc53f472ec2026-07-02Warnings, Adverse reactionsExact identifier
rxcui: 311347
unii: ISQ9I6J12J

Reported adverse events (FAERS/openFDA)#

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