FDA.reportPublic FDA data

NDC 17856-0678 - 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
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

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Phenobarbital - ATLANTIC BIOLOGICALS CORPATLANTIC BIOLOGICALS CORP2023-04-18Human Prescription Drug Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-0678-12025-01-30C16284748780-12cef2736-6049-d83d-e063-dadaa90ab31fPHENOBARBITAL ORAL SOLUTION, USP CIV
17856-0678-22025-01-30C16284748780-12cef2736-6049-d83d-e063-dadaa90ab31fPHENOBARBITAL ORAL SOLUTION, USP CIV
17856-0678-32025-01-30C16284748780-12cef2736-6049-d83d-e063-dadaa90ab31fPHENOBARBITAL ORAL SOLUTION, USP CIV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-0678-1Phenobarbital72 in 1 BOX, UNIT-DOSELIQUID721
17856-0678-2Phenobarbital72 in 1 BOX, UNIT-DOSELIQUID721
17856-0678-3Phenobarbital48 in 1 BOX, UNIT-DOSELIQUID481
17856-0678-4Phenobarbital5 mL in 1 CUP, UNIT-DOSELIQUID51
17856-0678-5Phenobarbital7.5 mL in 1 CUP, UNIT-DOSELIQUID7.51
17856-0678-6Phenobarbital5 mL in 1 SYRINGELIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0678PHENOBARBITAL LIQUID [ATLANTIC BIOLOGICALS CORP]16 package rows20230420_ac26cd10-8f66-4254-957c-87a909b576f8.zip