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 79 of 301 · 6,019 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
70% RubbingISOPROPYL ALCOHOLWalgreens Co.6ad37d18-5c19-4b5f-8313-edd430f84fb02026-02-05Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLWalgreens Co.1473e6e4-dc5f-43d9-a249-111a181e3f762026-02-05Warnings, Adverse reactionsExact identifier
unii: ND2M416302
ForPro Premium Sterile Antiseptic Isopropyl Alcohol PadsISOPROPYL ALCOHOLTng workdwide6cc2ccae-b288-473e-a736-0974c96dbb892026-02-05WarningsExact identifier
unii: ND2M416302
Hand Sanitizer Cherry PopALCOHOLScent Theory Products LLC4a18b475-fd3b-10a3-e063-6294a90a4f472026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Ocean SplashALCOHOLScent Theory Products LLC4a18d7b2-94ca-7924-e063-6394a90af3d12026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Banana CremeALCOHOLScent Theory Products LLC4a18e8e0-43e3-70d8-e063-6294a90adf4b2026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Juicy PearALCOHOLScent Theory Products LLC4a18e8e0-43e5-70d8-e063-6294a90adf4b2026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Pink MelonALCOHOLScent Theory Products LLC4a18ec9c-d466-63c1-e063-6294a90a11222026-02-05WarningsExact identifier
unii: 3K9958V90M
Isopropyl AlcoholISOPROPYL ALCOHOLPharmacy Value Alliance, LLC528011d7-8c6d-4940-bee1-52b39acef40d2026-02-05Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Advanced Hand SanitizerALCOHOLPublix Super Markets, Inc.11ef0139-940f-444d-a8f8-98f693ccff222026-02-05Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Isopropyl AlcoholISOPROPYL ALCOHOLPublix Super Markets, Inc.14aecc7b-c68a-4cb9-863f-475e204f66a52026-02-05WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLPublix Super Markets, Inc.b3b5324b-ee2c-4f87-9bb9-81d3d85f73ee2026-02-05WarningsExact identifier
unii: ND2M416302
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 BambooOCTINOXATE, TITANIUM DIOXIDEBCM Cosmetique SASebfe03e7-614f-44b1-b1f1-78edc7e274cc2026-02-05WarningsExact identifier
unii: 15FIX9V2JP
Hand Sanitizer 8 oz. Vitamin E 70 v/vETHYL ALCOHOLNingbo Rejoice Internationala26a6f97-7166-0a40-e053-2a95a90a4b682026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Vitamin E and Aloe VeraETHYL ALCOHOLNingbo Rejoice Internationala26a4676-6eae-088a-e053-2a95a90a7c1a2026-02-05WarningsExact identifier
unii: 3K9958V90M
Isopropyl alcohol 50 percentISOPROPYL ALCOHOLEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)b1b52183-3296-48b2-b3d3-821c141b0bea2026-02-05WarningsExact identifier
unii: ND2M416302
Isopropyl alcohol 50 percentISOPROPYL ALCOHOLEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)ee67fb96-fa2c-4542-8fdb-f2ccd885ee532026-02-05WarningsExact identifier
unii: ND2M416302
SHISEIDO URBAN ENVIRONMENT oil-free MINERAL SUNSCREEN SPF 42TITANIUM DIOXIDE AND ZINC OXIDESHISEIDO AMERICAS CORPORATION86630e82-f249-4866-82dd-3e21feb266c42026-02-04WarningsExact identifier
unii: 15FIX9V2JP
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMSportpharm LLC94b7c1bb-c024-4dc6-86d4-18a17a3eafcb2026-02-04Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Isopropyl AlcoholISOPROPYL ALCOHOLDyad Medical Sourcing, LLCb5c9e222-10eb-4cea-af70-213a77fcc8652026-02-04Warnings, Adverse reactionsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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