FDA.reportPublic FDA data

NDC 70518-0895-2 - Amoxicillin

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
70518-0895
Requested NDC
70518-0895-2
Package NDCs from labels
70518-0895-0, 70518-0895-2, 70518-0895-1, 70518-0895-3, 70518-0895-4, 70518-0895-5, 70518-0895-6, 70518-0895-7, 70518-0895-8, 70518-0895-9
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Amoxicillin - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-01HUMAN PRESCRIPTION DRUG LABEL
Amoxicillin - Sportpharm LLCSportpharm LLC2026-02-03HUMAN PRESCRIPTION DRUG LABEL
Amoxicillin - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEMAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2024-11-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-0895-0Amoxicillin30 in 1 BOTTLECAPSULE3018
70518-0895-1Amoxicillin100 in 1 BOXCAPSULE10018
70518-0895-2Amoxicillin1 in 1 POUCHCAPSULE118
70518-0895-3Amoxicillin21 in 1 BOTTLE, PLASTICCAPSULE2118
70518-0895-4Amoxicillin21 in 1 BOTTLE, PLASTICCAPSULE2118
70518-0895-5Amoxicillin30 in 1 BLISTER PACKCAPSULE3018
70518-0895-6Amoxicillin21 in 1 BLISTER PACKCAPSULE2118
70518-0895-7Amoxicillin28 in 1 BLISTER PACKCAPSULE2818
70518-0895-8Amoxicillin30 in 1 BOTTLE, PLASTICCAPSULE3018
70518-0895-9Amoxicillin20 in 1 BOTTLE, PLASTICCAPSULE2018

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-0895AMOXICILLIN CAPSULE [REMEDYREPACK INC.]16Current NDC, Legacy NDC, 10 package rows20250503_53548597-347b-42a9-916c-e88cd27b8dcd.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 96 of 119 · 2,365 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bare Republic Mineral Shimmer SPF 30 Diamond DustTITANIUM DIOXIDE, ZINC OXIDECOOLA, LLCeec83ecb-d0ab-7857-e053-2995a90a40ed2024-05-22WarningsExact identifier
unii: 15FIX9V2JP
AmoxicillinAMOXICILLINTeva Pharmaceuticals USA, Inc.4c0f348a-a65d-409c-8668-207c82a5e3cb2024-05-22Warnings, Adverse reactionsExact identifier
rxcui: 308182
rxcui: 308191
unii: 804826J2HU
Protective Tinted Moisturizer Broad Spectrum Sunscreen SPF 30TITANIUM DIOXIDE, ZINC OXIDEJune Jacobs Labs LLC18e1edd9-e39b-c91f-e063-6394a90a32a02024-05-20WarningsExact identifier
unii: 15FIX9V2JP
Mineral Sun Defense Moisturizer Broad Spectrum Sunscreen SPF 30TITANIUM DIOXIDE, ZINC OXIDEJune Jacobs Labs, LLC18e4c50d-eb91-c269-e063-6394a90a79992024-05-20WarningsExact identifier
unii: 15FIX9V2JP
Protectif UntintedZINC OXIDE AND TITANIUM DIOXIDEAllure Labs18aa2604-c8f0-ca04-e063-6294a90a1c252024-05-17WarningsExact identifier
unii: 15FIX9V2JP
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMA-S Medication Solutionsaaa35f65-cb9c-4b37-a126-c5ff2c2ef79d2024-05-16Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AugmentinAMOXICILLIN AND CLAVULANATE POTASSIUMAllegis Holdings, LLC04a31a42-d79e-bbb4-e063-6394a90a63ee2024-05-16Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMA-S Medication Solutions2718248d-d948-466e-959b-1a972519f1082024-05-14Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Jack BlackTITANIUM DIOXIDE, ZINC OXIDEJack Black L.L.C181d5bf3-ce91-cb2c-e063-6294a90a51c42024-05-10WarningsExact identifier
unii: 15FIX9V2JP
Protectif Fair TintZINC OXIDE AND TITANIUM DIOXIDEAllure Labs181e3f34-c5b2-0976-e063-6394a90a9a782024-05-10WarningsExact identifier
unii: 15FIX9V2JP
Protectif Deep TintZINC OXIDE AND TITANIUM DIOXIDEAllure Labs180b2939-5ae4-88fb-e063-6394a90aad932024-05-09WarningsExact identifier
unii: 15FIX9V2JP
AmoxicillinAMOXICILLINA-S Medication Solutions14a5f8c2-fdaf-4ad4-982b-c5aa128e242d2024-05-06Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
EnviroclenzBERBERIS VULGARIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, STILLINGIA SYLVATICA, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, GERMANIUM SESQUIOXIDE, PHYTOLACCA DECANDRA, ACETONE, AMMONIUM MURIATICUM, BENZINUM, PROPYLENE GLYCOL, SODIUM LAURYL SULFATE, SODIUM TRIPOLYPHOSPHATE, TEREBINTHINA, METHANOL, CHLORINUM, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUMDeseret Biologicals, Inc.92816bbe-96d6-45fc-9929-d3e6df394a332024-05-02WarningsExact identifier
unii: 368GB5141J
AmoxicillinAMOXICILLINA-S Medication Solutions7db086c6-a56b-4848-9eec-abaaff9f5b6f2024-05-01Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINA-S Medication Solutionsd5ecb620-5267-4dcf-be81-64c7766516f52024-05-01Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINA-S Medication Solutionsa2a5bb34-671b-499c-b8b4-c40fb51af09a2024-04-30Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINA-S Medication Solutions3d8a700b-b23b-459a-a19a-213dd39b6a3a2024-04-30Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINA-S Medication Solutionsefc66d77-1733-41e1-9aed-7c10a4b4ba962024-04-30Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AMOXICILLIN AND CLAVULANATE POTASSIUMAMOXICILLIN AND CLAVULANATE POTASSIUMA-S Medication Solutions00cf4429-e37c-4490-b22d-3cd7961242962024-04-30Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINA-S Medication Solutions6a3d1af5-6e93-4f06-8d82-1c87290c46aa2024-04-30Warnings, Adverse reactionsExact identifier
unii: 804826J2HU

Reported adverse events (FAERS/openFDA)#

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