PHENOBARBITAL

Product NDC
70752-162
11-digit product format
707520162
Labeler code
70752
Product ID
70752-162_234e0cf8-e1c9-47a2-8fa3-8a4db929c866
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PHENOBARBITAL
Dosage form
TABLET
Route
ORAL
Labeler
QUAGEN PHARMACEUTICALS LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-09-15
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 UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
YQE403BP4DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198086Internal RxNorm lookup
199164Internal RxNorm lookup
199167Internal RxNorm lookup
199168Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7e6853a4-478d-40e3-b041-4cff02a74c8cAvailable on FDA.report

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70752-162-10PHENOBARBITAL100 in 1 BOTTLETABLET1002
70752-162-11PHENOBARBITAL1000 in 1 BOTTLETABLET10002
70752-162-14PHENOBARBITAL500 in 1 BOTTLETABLET5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70752-162PHENOBARBITAL TABLET [QUAGEN PHARMACEUTICALS LLC]2Current NDC, Legacy NDC, 3 package rows20230217_7e6853a4-478d-40e3-b041-4cff02a74c8c.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PHENOBARBITALPHENOBARBITALQUAGEN PHARMACEUTICALS LLC7e6853a4-478d-40e3-b041-4cff02a74c8c2023-02-16Warnings, Adverse reactionsExact identifier
ndc (product): 70752-162

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198086PHENobarbital 16.2 MG Oral TabletPSN7e6853a4-478d-40e3-b041-4cff02a74c8c2
199167PHENobarbital 32.4 MG Oral TabletPSN7e6853a4-478d-40e3-b041-4cff02a74c8c2
199168PHENobarbital 64.8 MG Oral TabletPSN7e6853a4-478d-40e3-b041-4cff02a74c8c2
199164PHENobarbital 97.2 MG Oral TabletPSN7e6853a4-478d-40e3-b041-4cff02a74c8c2
198086phenobarbital 16.2 MG Oral TabletSCD7e6853a4-478d-40e3-b041-4cff02a74c8c2
199167phenobarbital 32.4 MG Oral TabletSCD7e6853a4-478d-40e3-b041-4cff02a74c8c2
199168phenobarbital 64.8 MG Oral TabletSCD7e6853a4-478d-40e3-b041-4cff02a74c8c2
199164phenobarbital 97.2 MG Oral TabletSCD7e6853a4-478d-40e3-b041-4cff02a74c8c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70752-162-1070752016210100 TABLET in 1 BOTTLE (70752-162-10) 100 tablet2020-09-150000-00-00NoNoCurrent
70752-162-11707520162111000 TABLET in 1 BOTTLE (70752-162-11) 1000 tablet2020-09-150000-00-00NoNoCurrent
70752-162-1470752016214500 TABLET in 1 BOTTLE (70752-162-14) 500 tablet2020-09-150000-00-00NoNoCurrent