Home NDC 43598-981-79 NDC 43598-981-79 - Rivaroxaban 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 43598-981
Requested NDC 43598-981-79
Package NDCs from labels 43598-981-60, 43598-981-18, 43598-981-79, 43598-981-78
Manufacturer Dr.Reddy's Laboratories, Inc. | Dr.Reddy's Laboratories Limited
Effective date 2026-04-29
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43598-981-18 Rivaroxaban 180 in 1 BOTTLE TABLET 180 11 43598-981-60 Rivaroxaban 60 in 1 BOTTLE TABLET 60 11 43598-981-78 Rivaroxaban 10 in 1 CARTON TABLET 10 11 43598-981-79 Rivaroxaban 10 in 1 BLISTER PACK TABLET 10 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43598-981 RIVAROXABAN TABLET [DR.REDDY'S LABORATORIES, INC.] 9 Current NDC, 4 package rows 20250515_122e6f78-067b-9065-adb2-ec7fec9f008e.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 5 of 109 · 2,180 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.