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 67 of 301 · 6,019 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Anti Bacterial Hand Gel WinterALCOHOLBath & Body Works, Inc.46136f12-b335-98c2-e063-6294a90a00af2026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Snowflakes and CashmereALCOHOLBath & Body Works, Inc.4604db79-ddbe-c83d-e063-6394a90aadd82026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Honey WildflowerALCOHOLBath & Body Works, Inc.46153052-5e6e-b8d3-e063-6294a90a60fc2026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel FreshwaterALCOHOLBath & Body Works, Inc.4613a872-0967-c800-e063-6394a90a22d02026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Pink Bubble GumALCOHOLBath & Body Works, Inc.4614de38-80f8-26db-e063-6294a90ab4f82026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Winterberry IceALCOHOLBath & Body Works, Inc.46138a35-e974-a8bb-e063-6394a90a5b542026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel AdrenalineALCOHOLBath & Body Works, Inc.4613bfd7-77ff-e237-e063-6394a90ad3d62026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel Fiji White SandsALCOHOLBath & Body Works, Inc.461420e0-a5b1-81df-e063-6394a90a94ec2026-03-09WarningsExact identifier
unii: 3K9958V90M
Anti Bacterial Hand Gel WinterALCOHOLBath & Body Works, Inc.4613ce33-6881-e7c8-e063-6394a90a40902026-03-09WarningsExact identifier
unii: 3K9958V90M
Natouch Antifungal Antiseptic WipesANTIFUNGAL ANTISEPTIC WIPESNatouch LLC4c84c556-8d0b-ec28-e063-6294a90af1d32026-03-08WarningsExact identifier
unii: 3K9958V90M
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMAmerican Health Packaging4966a3f2-eed2-4081-ba88-310a3d1964b42026-03-06Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
2-Pack Facial Serum2-PACK FACIAL SERUMGuangzhou Ariel Biotech Co., Ltd.27c7f645-cfb3-6db1-e063-6394a90a42ff2026-03-06WarningsExact identifier
unii: 059QF0KO0R
MediChoice Antiseptic Isopropyl Alcohol Prep PadsISOPROPYL ALCOHOLO&M HALYARD, INC.20b3694e-04c7-4bca-b2ce-62ae0dec7a832026-03-05WarningsExact identifier
unii: ND2M416302
MediChoice Alcohol SwabstickISOPROPYL ALCOHOLO&M HALYARD, INC.7f78529d-df17-44b3-a890-1afa35308c672026-03-05WarningsExact identifier
unii: ND2M416302
MediChoice Alcohol Prep PadsISOPROPYL ALCOHOLO&M HALYARD, INC.f4f54448-0de0-448c-9b7b-104370953ae52026-03-05WarningsExact identifier
unii: ND2M416302
MediChoice Alcohol SwabstickISOPROPYL ALCOHOLO&M HALYARD, INC.7cee1141-4a49-4fec-a627-91a88e3d3ffc2026-03-05WarningsExact identifier
unii: ND2M416302
cle de peau BEAUTE RADIANT FLUID FOUNDATION NATURAL B50OCTINOXATE AND TITANIUM DIOXIDESHISEIDO AMERICAS CORPORATION4490f968-46b6-44d2-af2d-5130b52c88612026-03-05WarningsExact identifier
unii: 15FIX9V2JP
SPA HAND SANITIZER WRTER MELON SPLASHETHYL ALCOHOLRejoice International Corp.4c53620d-01ee-8ddd-e063-6294a90a8a2b2026-03-05WarningsExact identifier
unii: 3K9958V90M
Smart Care PISTACHIO CREME HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.e763a268-b8d0-4237-bf8e-28433c0e80b22026-03-05WarningsExact identifier
unii: 3K9958V90M
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMPreferred Pharmaceuticals Inc.fc31a5df-aa1c-4b0f-8c64-a14236df4a022026-03-05Warnings, Adverse reactionsExact identifier
unii: 804826J2HU

Reported adverse events (FAERS/openFDA)#

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