Home NDC 69339-150-01 NDC 69339-150-01 - Guaifenesin Syrup and Dextromethorphan 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 69339-150
Requested NDC 69339-150-01
Package NDCs from labels 69339-150-01, 69339-150-19
Manufacturer Natco Pharma USA LLC
Effective date 2023-11-01
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 69339-150-01 Guaifenesin Syrup and Dextromethorphan 10 mL in 1 CUP, UNIT-DOSE SYRUP 10 6 69339-150-19 Guaifenesin Syrup and Dextromethorphan 10 in 1 TRAY SYRUP 10 6 69339-150-19 Guaifenesin Syrup and Dextromethorphan 10 in 1 CASE SYRUP 10 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69339-150 GUAIFENESIN SYRUP AND DEXTROMETHORPHAN SYRUP [NATCO PHARMA USA LLC] 6 Current NDC, Legacy NDC, 3 package rows 20231102_ad9026f4-f0b6-4d02-aa44-f0460eeefc0e.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 102 of 318 · 6,346 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.