Home NDC 70518-3733-01 NDC 70518-3733-01 - Celecoxib 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 70518-3733
Requested NDC 70518-3733-01
Package NDCs from labels 70518-3733-0, 70518-3733-1, 70518-3733-2, 70518-3733-3, 70518-3733-4, 70518-3733-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-08-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Celecoxib - REMEDYREPACK INC. REMEDYREPACK INC. 2026-08-17 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-3733-0 Celecoxib 45 in 1 BOTTLE, PLASTIC CAPSULE 45 8 70518-3733-1 Celecoxib 30 in 1 BOTTLE, PLASTIC CAPSULE 30 8 70518-3733-2 Celecoxib 90 in 1 BOTTLE, PLASTIC CAPSULE 90 8 70518-3733-3 Celecoxib 60 in 1 BOTTLE, PLASTIC CAPSULE 60 8 70518-3733-4 Celecoxib 14 in 1 BOTTLE, PLASTIC CAPSULE 14 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-3733 CELECOXIB CAPSULE [REMEDYREPACK INC.] 6 Current NDC, 5 package rows 20241127_b3acbfd9-a1c2-4aa6-b5f0-013cfad6cca8.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 108 of 115 · 2,284 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.