Home NDC 17856-0138-01 NDC 17856-0138-01 - Lidocaine hydrochloride 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 17856-0138
Requested NDC 17856-0138-01
Package NDCs from labels 17856-0138-3, 17856-0138-1, 17856-0138-4, 17856-0138-2, 17856-0138-6, 17856-0138-5, 17856-0138-01
Manufacturer ATLANTIC BIOLOGICALS CORP.
Effective date 2025-05-12
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 17856-0138-1 Lidocaine hydrochloride 50 in 1 BOX, UNIT-DOSE SOLUTION 50 3 17856-0138-2 Lidocaine hydrochloride 50 in 1 BOX, UNIT-DOSE SOLUTION 50 3 17856-0138-3 Lidocaine hydrochloride 15 mL in 1 CUP, UNIT-DOSE SOLUTION 15 3 17856-0138-4 Lidocaine hydrochloride 20 mL in 1 CUP, UNIT-DOSE SOLUTION 20 3 17856-0138-5 Lidocaine hydrochloride 72 in 1 BOX, UNIT-DOSE SOLUTION 72 3 17856-0138-6 Lidocaine hydrochloride 5 mL in 1 CUP, UNIT-DOSE SOLUTION 5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17856-0138 LIDOCAINE HYDROCHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.] 3 Current NDC, 6 package rows 20250514_75d17334-6876-42d0-8a02-82669d139e4f.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 16 of 48 · 941 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.