Home NDC 70518-2191-01 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 Label Manufacturer Effective date Type Amoxicillin - REMEDYREPACK INC. REMEDYREPACK INC. 2026-07-21 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-2191-0 Amoxicillin 20 in 1 BLISTER PACK TABLET, FILM COATED 20 16 70518-2191-1 Amoxicillin 30 in 1 BLISTER PACK TABLET, FILM COATED 30 16 70518-2191-2 Amoxicillin 20 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 20 16 70518-2191-3 Amoxicillin 14 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 14 16 70518-2191-4 Amoxicillin 14 in 1 BLISTER PACK TABLET, FILM COATED 14 16
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-2191 AMOXICILLIN TABLET, FILM COATED [REMEDYREPACK INC.] 14 Current NDC, Legacy NDC, 5 package rows 20250309_9618d038-e880-47f6-b8d7-bbf8ab35364d.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 138 of 152 · 3,030 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.