PHENOBARBITAL

Product NDC
70752-157
11-digit product format
707520157
Labeler code
70752
Product ID
70752-157_186052cb-c8b2-4d33-a04e-7538302c9c66
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PHENOBARBITAL
Dosage form
SOLUTION
Route
ORAL
Labeler
QUAGEN PHARMACEUTICALS LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-08-03
Marketing end
0000-00-00
Substance
PHENOBARBITAL
Active strength
20 mg/5mL
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct70752-157IInactivated by FDA2026-10-12
excluded packagepackage70752-15770752-157-12IInactivated by FDA2026-10-12

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e3e67a66-d325-4d80-8f9d-059e736d7b00Product name120230912

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70752-157-122023-02-02C16284748780-1f386c649-f080-0266-e053-dadaa90a7c1aPHENOBARBITAL ORAL SOLUTION, USP CIV Rx only
70752-157-122023-01-30C16284748780-1f386c649-f080-0266-e053-dadaa90a7c1aPHENOBARBITAL ORAL SOLUTION, USP CIV Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70752-157-12PHENOBARBITAL473 mL in 1 BOTTLESOLUTION4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70752-157PHENOBARBITAL SOLUTION [QUAGEN PHARMACEUTICALS LLC]2Legacy NDC, 1 package rows20230203_f96c7937-4968-4e14-b2f0-0dd5f79ae841.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
702519PHENobarbital 20 MG in 5 mL Oral SolutionPSNf96c7937-4968-4e14-b2f0-0dd5f79ae8412
702519phenobarbital 4 MG/ML Oral SolutionSCDf96c7937-4968-4e14-b2f0-0dd5f79ae8412
702519phenobarbital 20 MG per 5 ML Oral SolutionSYf96c7937-4968-4e14-b2f0-0dd5f79ae8412
702519phenobarbital 30 MG per 7.5 ML Oral SolutionSYf96c7937-4968-4e14-b2f0-0dd5f79ae8412
702519phenobarbital 60 MG per 15 ML Oral SolutionSYf96c7937-4968-4e14-b2f0-0dd5f79ae8412

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70752-157-1270752015712473 mL in 1 BOTTLE (70752-157-12) 473 ml2020-08-030000-00-00NoNoCurrent