Phenobarbital

Product NDC
67296-2145
11-digit product format
672962145
Labeler code
67296
Product ID
67296-2145_4637fbff-2c91-27f6-e063-6394a90a886f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenobarbital
Dosage form
TABLET
Route
ORAL
Labeler
Redpharm Drug
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2023-09-08
Substance
PHENOBARBITAL
Active strength
32.4 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Phenobarbital
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENOBARBITAL32.4 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiYQE403BP4D
Rxcui199167

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-2145-2Phenobarbital20 in 1 BOTTLETABLET204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67296-2145PHENOBARBITAL TABLET [REDPHARM DRUG]1Current NDC, 1 package rows20250410_3252a6bb-02e8-7992-e063-6394a90aec3d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199167PHENobarbital 32.4 MG Oral TabletPSN3252a6bb-02e8-7992-e063-6394a90aec3d4
199167phenobarbital 32.4 MG Oral TabletSCD3252a6bb-02e8-7992-e063-6394a90aec3d4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
67296-2145-26729621450220 TABLET in 1 BOTTLE (67296-2145-2) 20 tablet2023-09-08NoNoCurrent