Phenobarbital

Product NDC: 72162-1168
Requested package NDC: 72162-1168-0
11-digit product format: 721621168
Labeler code: 72162
Product ID: 72162-1168_10734a98-e252-4514-9cc4-afe27d8ee2d8
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: phenobarbital
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2001-12-01
Substance: PHENOBARBITAL
Active strength: 97.2 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	97.2 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
199164	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
1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6	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
72162-1168-0	Phenobarbital	1000 in 1 BOTTLE, PLASTIC	TABLET	1000		101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72162-1168-0	EA - Each	72162-1168	881f144c-475a-40fc-b0c8-46582aff3d4e	1	2024-05-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72162-1168	PHENOBARBITAL TABLET [BRYANT RANCH PREPACK]	101	Current NDC, 1 package rows	20241018_1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6.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	1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6	2024-10-04	Warnings, Adverse reactions	Exact identifier ndc (package): 72162-1168-0 ndc (product): 72162-1168 ndc11 (package): 72162116800

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
199164	PHENobarbital 97.2 MG Oral Tablet	PSN	1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6	101
199164	phenobarbital 97.2 MG Oral Tablet	SCD	1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6	101

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72162-1168-0	72162116800	1000 TABLET in 1 BOTTLE, PLASTIC (72162-1168-0)	1000 tablet	2001-12-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Phenobarbital Tablets, USP CIV Rx only	Bryant Ranch Prepack	2024-10-04	HUMAN PRESCRIPTION DRUG LABEL	101