Home NDC 17856-0678-4 NDC 17856-0678-4 - Phenobarbital 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 17856-0678
Requested NDC 17856-0678-4
Package NDCs from labels 17856-0678-4, 17856-0678-1, 17856-0678-5, 17856-0678-2, 17856-0678-6, 17856-0678-3
Manufacturer ATLANTIC BIOLOGICALS CORP
Effective date 2023-04-18
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 17856-0678-1 Phenobarbital 72 in 1 BOX, UNIT-DOSE LIQUID 72 1 17856-0678-2 Phenobarbital 72 in 1 BOX, UNIT-DOSE LIQUID 72 1 17856-0678-3 Phenobarbital 48 in 1 BOX, UNIT-DOSE LIQUID 48 1 17856-0678-4 Phenobarbital 5 mL in 1 CUP, UNIT-DOSE LIQUID 5 1 17856-0678-5 Phenobarbital 7.5 mL in 1 CUP, UNIT-DOSE LIQUID 7.5 1 17856-0678-6 Phenobarbital 5 mL in 1 SYRINGE LIQUID 5 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17856-0678 PHENOBARBITAL LIQUID [ATLANTIC BIOLOGICALS CORP] 1 6 package rows 20230420_ac26cd10-8f66-4254-957c-87a909b576f8.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 13 of 168 · 3,348 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.