Home NDC 17856-0182-2 NDC 17856-0182-2 - ACETAMINOPHEN 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 17856-0182
Requested NDC 17856-0182-2
Package NDCs from labels 17856-0182-2, 17856-0182-1, 17856-0182-3, 17856-0182-5, 17856-0182-4
Manufacturer ATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONS
Effective date 2022-11-14
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17856-0182-1 ACETAMINOPHEN 120 in 1 BOX, UNIT-DOSE ELIXIR 120 3 17856-0182-2 ACETAMINOPHEN 2 mL in 1 SYRINGE ELIXIR 2 3 17856-0182-3 ACETAMINOPHEN 5 in 1 SYRINGE ELIXIR 5 3 17856-0182-4 ACETAMINOPHEN 72 in 1 BOX, UNIT-DOSE ELIXIR 72 3 17856-0182-5 ACETAMINOPHEN 5 mL in 1 CUP, UNIT-DOSE ELIXIR 5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17856-0182 ACETAMINOPHEN ELIXIR [ATLANTIC BIOLOGICALS CORP.] 3 Legacy NDC, 5 package rows 20221115_cf2dd95d-afea-462d-9dba-a46a68bf67e6.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 67 of 182 · 3,635 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.