NDC 0143-9575-01 - Lidocaine

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
0143-9575
Requested NDC
0143-9575-01
Package NDCs from labels
0143-9575-01, 0143-9575-10
Manufacturer
A-S Medication Solutions
Effective date
2025-10-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lidocaine - A-S Medication SolutionsA-S Medication Solutions2025-10-21HUMAN PRESCRIPTION DRUG LABEL
LIDOCAINE HCI - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2025-07-09HUMAN PRESCRIPTION DRUG LABEL
Lidocaine - Hikma Pharmaceuticals USA Inc.Hikma Pharmaceuticals USA Inc.2025-05-01HUMAN PRESCRIPTION DRUG LABEL
Lidocaine - Medical Purchasing Solutions, LLCMedical Purchasing Solutions, LLC2023-05-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0143-9575-01Lidocaine50 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION506
0143-9575-10Lidocaine10 in 1 PACKAGEINJECTION, SOLUTION106

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0143-9575LIDOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION LIDOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HIKMA PHARMACEUTICALS USA INC.]5Current NDC, Legacy NDC, 2 package rows20250521_5523fdfe-69fd-49a5-b51f-73e2223d49a9.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9575-01ML - Milliliter0143-9575e0e5c666-8931-44d8-b700-5faf7af1888012017-10-13
0143-9575-10ML - Milliliter0143-957523cc4249-984a-418e-a4b5-e58307ead77412017-10-13

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 61 of 79 · 1,567 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine Hydrochloride and Hydrocortisone AcetateLIDOCAINE HYDROCHLORIDE AND HYDROCORTISONE ACETATESeton Pharmaceuticals951862db-3a73-4d25-9d5b-e4111833f43b2024-01-30Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine Hydrochloride and Hydrocortisone AcetateLIDOCAINE HYDROCHLORIDE AND HYDROCORTISONE ACETATESeton Pharmaceuticals6aa284d6-0212-4fb5-809d-c721aa6fe2ba2024-01-30Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LIDOCAINE HCILIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst993bc59e-5e71-bd9e-e053-2a95a90af85c2024-01-28Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
2% LIDOCAINE HCI2% LIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst78d8fb0a-bfae-6599-e053-2991aa0a2e032024-01-28Warnings, Adverse reactionsExact identifier
rxcui: 1010671
unii: V13007Z41A
LIDOCAINE HClLIDOCAINE HCLHF Acquisition Co LLC, DBA HealthFirstc4c16714-6b1f-857e-e053-2a95a90a74e42024-01-28Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
XYLOCAINEXYLOCAINEHF Acquisition Co LLC, DBA HealthFirste3b3b462-8f35-68b8-e053-2995a90a64032024-01-27Warnings, Adverse reactionsExact identifier
rxcui: 1010033
LACTATED RINGERSSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirsta14ca7d9-de30-a303-e053-2a95a90a53042024-01-27Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
LIDOCAINE HCILIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirstc901016e-9293-79dd-e053-2a95a90a0fda2024-01-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LIDOCAINE HClLIDOCAINE HCLHF Acquisition Co LLC, DBA HealthFirste8bc96bc-7876-4906-e053-2a95a90ae6ba2024-01-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LIDOCAINE HClLIDOCAINE HCLHF Acquisition Co LLC, DBA HealthFirste39435a3-1f69-78c5-e053-2995a90a7fc32024-01-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
0.5% LIDOCAINE HCl0.5% LIDOCAINE HCLHF Acquisition Co LLC, DBA HealthFirste52fe254-8872-35ce-e053-2a95a90a339e2024-01-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
0.9% SODIUM CHLORIDE0.9% SODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirste5247ed5-6170-c13f-e053-2a95a90a41012024-01-27Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Target Up and Up Pain Relieving CleansingBENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDETARGET CORPORATION0f964747-be02-c715-e063-6294a90ad91e2024-01-25WarningsExact identifier
unii: V13007Z41A
LIDOCAINE HCILIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst95351883-ec37-f94a-e053-2995a90aa36a2024-01-25Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
BSSBALANCED SALT SOLUTIONAlcon Laboratories, Inc.4bd4d59c-eb3b-4a5e-9eb7-ae95b0a92bea2024-01-25Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
CIRCULATION HPARNICA MONTANA, AURUM METALLICUM, CACTUS GRANDIFLORUS, CALCAREA CARBONICA, LACHESIS MUTUS, NATRUM MURIATICUM, NUX VOMICA, PHOSPHORUS, SOLIDAGO VIRGAUREA,Energique, Inc.464d208b-3893-4ec6-9868-12ef6807b98d2024-01-23WarningsExact identifier
unii: 451W47IQ8X
DERMA SCALE HPARSENICUM IODATUM, BORAX, GRAPHITES, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PETROLEUM, SEPIA, SULPHUREnergique, Inc.64961787-7e9a-4e6f-98ce-0f51934155cf2024-01-23WarningsExact identifier
unii: 451W47IQ8X
Burn First AidBURN FIRST AIDDynarex Corporation826e08be-dffa-5a27-e053-2a91aa0a87012024-01-22WarningsExact identifier
unii: V13007Z41A
LIDOCAINE HCILIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst995e68a7-6986-423e-e053-2995a90acd982024-01-22Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
XYLOCAINEXYLOCAINEHF Acquisition Co LLC, DBA HealthFirst0c6c5678-e987-b822-e063-6394a90ac88b2024-01-22Warnings, Adverse reactionsExact identifier
rxcui: 1010033

Reported adverse events (FAERS/openFDA)#

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