Phenobarbital

Product NDC: 63629-2401
11-digit product format: 636292401
Labeler code: 63629
Product ID: 63629-2401_5500b038-6256-4d72-9ca3-a94d2a9dd664
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phenobarbital
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-11-01
Substance: PHENOBARBITAL
Active strength: 16.2 mg/1
DEA schedule: CIV
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PHENOBARBITAL	16.2 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
YQE403BP4D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198086	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
e1709a49-ee44-4679-9a57-a7ea85a78ab7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e3e67a66-d325-4d80-8f9d-059e736d7b00	Product name	1	20230912

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63629-2401-1	Phenobarbital	100 in 1 BOTTLE	TABLET	100		102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63629-2401-1	EA - Each	63629-2401	2ea5cc21-887e-4753-98b2-661820e225f0	1	2021-04-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63629-2401	PHENOBARBITAL TABLET [BRYANT RANCH PREPACK]	102	Current NDC, Legacy NDC, 1 package rows	20240112_e1709a49-ee44-4679-9a57-a7ea85a78ab7.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Phenobarbital	PHENOBARBITAL	Bryant Ranch Prepack	e1709a49-ee44-4679-9a57-a7ea85a78ab7	2024-01-11	Warnings, Adverse reactions	Exact identifier ndc (product): 63629-2401

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
YQE403BP4D	PHENOBARBITAL	50-06-6	PHENOBARBITAL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198086	PHENobarbital 16.2 MG Oral Tablet	PSN	e1709a49-ee44-4679-9a57-a7ea85a78ab7	102
198086	phenobarbital 16.2 MG Oral Tablet	SCD	e1709a49-ee44-4679-9a57-a7ea85a78ab7	102

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-2401-1	63629240101	100 TABLET in 1 BOTTLE (63629-2401-1)	100 tablet	2021-02-23	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PHENOBARBITAL TABLETS, USP C-IV Rx only WARNING: MAY BE HABIT-FORMING	Bryant Ranch Prepack	2024-01-11	HUMAN PRESCRIPTION DRUG LABEL	102