NDC 70518-2190-01 - 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
70518-2190
Requested NDC
70518-2190-01
Package NDCs from labels
70518-2190-0, 70518-2190-1, 70518-2190-2, 70518-2190-3, 70518-2190-4, 70518-2190-5, 70518-2190-6, 70518-2190-7, 70518-2190-8, 70518-2190-9, 70518-2190-01
Manufacturer
Sportpharm LLC
Effective date
2026-09-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Amoxicillin - Sportpharm LLCSportpharm LLC2026-09-29HUMAN PRESCRIPTION DRUG LABEL
Amoxicillin - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2190-0Amoxicillin28 in 1 BLISTER PACKCAPSULE2820
70518-2190-1Amoxicillin21 in 1 BLISTER PACKCAPSULE2120
70518-2190-2Amoxicillin30 in 1 BLISTER PACKCAPSULE3020
70518-2190-3Amoxicillin30 in 1 BOTTLE, PLASTICCAPSULE3020
70518-2190-4Amoxicillin21 in 1 BOTTLE, PLASTICCAPSULE2120
70518-2190-5Amoxicillin20 in 1 BOTTLE, PLASTICCAPSULE2020
70518-2190-6Amoxicillin1 in 1 POUCHCAPSULE120
70518-2190-7Amoxicillin100 in 1 BOXCAPSULE10020
70518-2190-8Amoxicillin14 in 1 BOTTLE, PLASTICCAPSULE1420
70518-2190-9Amoxicillin40 in 1 BOTTLE, PLASTICCAPSULE4020

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2190AMOXICILLIN CAPSULE [REMEDYREPACK INC.]14Current NDC, Legacy NDC, 10 package rows20250309_102c62ca-da20-4866-84a8-e3513824af4a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-2190-0EA - Each70518-2190b6fab721-38de-48cf-a1aa-b1f5c9bbd74912026-01-08
70518-2190-1EA - Each70518-2190dc54739d-9e6e-469e-8082-8adee5e1abf812026-01-08
70518-2190-2EA - Each70518-21907238c2f1-7aa1-4869-89b5-776bea1e2d0912026-01-08
70518-2190-3EA - Each70518-2190989cfed3-0e5f-4206-97f4-bacd0bdc97a512026-01-08
70518-2190-4EA - Each70518-21908efd7b8a-e169-4021-a191-d6de7b509f0312026-01-08
70518-2190-5EA - Each70518-2190cf968363-6064-434e-9bb9-a0cf8cea9e2512026-01-08

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 78 of 301 · 6,019 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ethyl Rubbing AlcoholETHYL ALCOHOLWalgreen Co.a08ef11f-5c4f-4821-a0c0-d6c89def0bea2026-02-10Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.800f5fac-f2af-358f-e053-2a91aa0ad6a62026-02-10Warnings, Adverse reactionsExact identifier
rxcui: 308191
unii: 804826J2HU
70%ISOPROPYL ALCOHOLWalgreen Co.fb918e7a-1fe0-4cfd-8cf0-9d823eb56dcc2026-02-10Warnings, Adverse reactionsExact identifier
unii: ND2M416302
MedlineISOPROPYL ALCOHOLHy-Vee, Inc.4bbce274-1e62-0c6a-e063-6394a90af92f2026-02-10WarningsExact identifier
unii: ND2M416302
Smart Care JAPANESE CHERRY BLOSSOM HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.bd25ab3b-d91e-4e61-a574-d0ec9037c41f2026-02-10WarningsExact identifier
unii: 3K9958V90M
Alumier MD Clear Shield Broad Spectrum SPF 42 SunscreenTITANIUM DIOXIDE, ZINC OXIDEAlumier Labsa9c970c8-b6e3-b0a1-e053-2a95a90a89c72026-02-09WarningsExact identifier
unii: 15FIX9V2JP
Droptics Performance Eye DropsNAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOLDroptics LLC20fd6822-a7fd-4593-92bb-0a07260893e22026-02-09WarningsExact identifier
unii: 6DC9Q167V3
Youmi Alcohol Prep Pad 70 Isopropyl AlcoholISOPROPYL ALCOHOLPT YOUMI MEDIKA INDUSTRIe3b1a576-a8eb-44bf-8f9c-a49a44a894e82026-02-09WarningsExact identifier
unii: ND2M416302
EVERLIT CARE PRODUCTS PREP PADISOPROPYL ALCOHOLEVERLIT GLOBAL INC.77a60360-8bb5-43e9-b7e4-f71d2d488c442026-02-09WarningsExact identifier
unii: ND2M416302
Everlit Care Products Sting ReliefISOPROPYL ALCOHOLEVERLIT GLOBAL INC.adfab206-b7de-4f6a-a864-edd946ea743d2026-02-09WarningsExact identifier
unii: ND2M416302
AlcoholISOPROPYL ALCOHOLA-S Medication Solutions6b8834be-0235-4f7c-8d52-c2f6aa2d30492026-02-08WarningsExact identifier
unii: ND2M416302
Hampton Sun SPF 50 MineralZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00%S&C Hampton Sun LLCd6c33436-042e-44e8-8b55-98be6e2468792026-02-06WarningsExact identifier
unii: 15FIX9V2JP
SHISEIDO WASO COLOR-SMART DAY MOISTURIZEROCTINOXATE, TITANIUM DIOXIDEShiseido Americas Corporationf291f077-1c72-48fc-bb19-c20bdeaaa5962026-02-06WarningsExact identifier
unii: 15FIX9V2JP
Hand SanitizerALCOHOLRetail Business Services, LLC8ba8176f-ddbd-48d7-bb62-74a499ea667c2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Advanced Hand SanitizerETHYL ALCOHOLRetail Business Services, LLC135ae232-3be4-4bbe-98fd-65eef3a675ad2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
SHISEIDO WASO COLOR-SMART DAY MOISTURIZEROCTINOXATE, TITANIUM DIOXIDEShiseido Americas Corporation54f63dd8-e77f-42e4-a6d3-61ab7beecf502026-02-06WarningsExact identifier
unii: 15FIX9V2JP
Advanced Hand SanitizerALCOHOLSalado Sales Inc.2869f574-e74c-492c-b3fa-b256b468746b2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMA-S Medication Solutions2a376d67-0bf2-43a1-8ca3-73f90689c3392026-02-06Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
SEYTU Body SunscreenTITANIUM DIOXIDE AND ZINC OXIDEOmnilife USA, Inc.c411e9a6-b2ea-446b-a886-b92c61736e6c2026-02-05WarningsExact identifier
unii: 15FIX9V2JP
SEYTU Facial SunscreenTITANIUM DIOXIDE AND ZINC OXIDEOmnilife USA, Inc.96fd37fb-c3ff-413f-b2c8-50754f320ecc2026-02-05WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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