FDA.reportPublic FDA data

NDC 70518-2191-01 - 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
70518-2191
Requested NDC
70518-2191-01
Package NDCs from labels
70518-2191-0, 70518-2191-1, 70518-2191-2, 70518-2191-3, 70518-2191-4, 70518-2191-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-21
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.2026-07-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2191-0Amoxicillin20 in 1 BLISTER PACKTABLET, FILM COATED2016
70518-2191-1Amoxicillin30 in 1 BLISTER PACKTABLET, FILM COATED3016
70518-2191-2Amoxicillin20 in 1 BOTTLE, PLASTICTABLET, FILM COATED2016
70518-2191-3Amoxicillin14 in 1 BOTTLE, PLASTICTABLET, FILM COATED1416
70518-2191-4Amoxicillin14 in 1 BLISTER PACKTABLET, FILM COATED1416

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2191AMOXICILLIN TABLET, FILM COATED [REMEDYREPACK INC.]14Current NDC, Legacy NDC, 5 package rows20250309_9618d038-e880-47f6-b8d7-bbf8ab35364d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-2191-1EA - Each70518-219180304746-448c-448e-bec0-25b5d3865dac12026-01-08
70518-2191-2EA - Each70518-21913b38d850-848c-404b-a49a-fb9487dfb0d812026-01-08
70518-2191-3EA - Each70518-219111d546b2-3544-4211-8b6c-2965d628c23f12026-01-08
70518-2191-4EA - Each70518-21916be8b8d2-5362-4a08-9599-ee67df270b9312026-01-08

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 117 of 152 · 3,030 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Reno Broad Spectrum SPF 25 SunscreenOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Incbe2a83fb-e4f8-4313-b5bd-150f351fb3452024-06-26WarningsExact identifier
unii: 15FIX9V2JP
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Reno Broad Spectrum SPF 25 SunscreenOCTINOXATE AND TITANIUM DIOXIDESICOS ET CIE066a0951-2e7e-40c0-8035-4d708a32f16c2024-06-26WarningsExact identifier
unii: 15FIX9V2JP
Yves Saint Laurent All Hours Foundation Broad Spectrum SPF 30 Sunscreen Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDESICOS ET CIE66a91768-6012-485a-b569-a293ea6d48802024-06-24WarningsExact identifier
unii: 15FIX9V2JP
Yves Saint Laurent All Hours Foundation Broad Spectrum SPF 30 Sunscreen Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Inc43539766-2e70-4b42-b64b-1d30367b2eb92024-06-24WarningsExact identifier
unii: 15FIX9V2JP
Exel Clarifying Line SPF 50OCTINOXATE, OCTOCRYLENE, OXYBENZONE, TATANIUM DIOXIDEBiocosmetica Exel Argentina SRLe65a68f6-d1b7-4cbf-a3f8-5cc04036221a2024-06-23WarningsExact identifier
unii: 15FIX9V2JP
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.997650f9-7eff-64de-e053-2995a90a617b2024-06-20Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMNuCare Pharmaceuticals,Inc.a0ff848d-230a-ab6b-e053-2a95a90a8bb82024-06-20Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINAurobindo Pharma Limited99103779-6d2f-4e4b-9b7f-0b24d7c6bf4e2024-06-20Warnings, Adverse reactionsExact identifier
application number: ANDA065256
ndc (product): 65862-015
rxcui: 308192
rxcui: 308194
spl id: ee0e12cd-e881-4048-a0fb-74bd771cb9aa
spl set id: 99103779-6d2f-4e4b-9b7f-0b24d7c6bf4e
unii: 804826J2HU
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMNuCare Pharmaceuticals,Inc.9263495c-310a-c20e-e053-2995a90a2e872024-06-19Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.97a657a3-8238-f5f1-e053-2a95a90a7a7a2024-06-19Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8c3ba9cf-9a28-3965-e053-2a95a90a38ce2024-06-18Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8dba39df-5df8-31aa-e053-2a95a90adae12024-06-18Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Protectif Fair TintZINC OXIDE AND TITANIUM DIOXIDEDerma Research Group Inc.1a8c8804-1d6b-b5a5-e063-6394a90a12602024-06-18WarningsExact identifier
unii: 15FIX9V2JP
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8398f2c9-37ca-9b59-e053-2991aa0a2c112024-06-14Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8995ac88-a094-2d16-e053-2a95a90a9a262024-06-14Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8af9b9ee-8a64-53f5-e053-2a95a90a62a42024-06-14Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINNuCare Pharmaceuticals,Inc.8c3dd74c-872a-1ba1-e053-2a95a90a7cb32024-06-13Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
Protectif UntintedZINC OXIDE AND TITANIUM DIOXIDEDerma Research Group Inc.1acd3f09-87f2-75e4-e063-6394a90a0cd92024-06-13WarningsExact identifier
unii: 15FIX9V2JP
Amoxicillin and Clavulanate PotassiumAMOXICILLIN AND CLAVULANATE POTASSIUMAsclemed USA, Inc.a94cfba3-27ed-46a3-81ef-e9b80187c2072024-06-13Warnings, Adverse reactionsExact identifier
unii: 804826J2HU
AmoxicillinAMOXICILLINAurobindo Pharma Limited3cacd754-73f4-496e-a529-9ca39fa6692d2024-06-13Warnings, Adverse reactionsExact identifier
unii: 804826J2HU

Reported adverse events (FAERS/openFDA)#

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