Phenobarbital Sodium

Product NDC: 71335-2993
11-digit product format: 713352993
Labeler code: 71335
Product ID: 71335-2993_131b9f89-35ac-4e38-b2c1-0180c0fbdf0b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phenobarbital Sodium
Dosage form: INJECTION
Route: INTRAMUSCULAR
Labeler: Bryant Ranch Prepack
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-02-05
Substance: PHENOBARBITAL SODIUM
Active strength: 130 mg/mL
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 Sodium
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PHENOBARBITAL SODIUM	130 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SW9M9BB5K3	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
312370	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
94673663-cf49-42ad-a201-09195b8d4e5b	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
71335-2993-1	Phenobarbital Sodium	25 in 1 BOX, UNIT-DOSE	INJECTION	25		100
71335-2993-2	Phenobarbital Sodium	1 mL in 1 VIAL	INJECTION	1		100

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71335-2993-1	ML - Milliliter	71335-2993	2175ee52-c26e-493c-b54a-82a153e8ee3a	1	2026-01-08

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 Sodium	PHENOBARBITAL SODIUM	Bryant Ranch Prepack	94673663-cf49-42ad-a201-09195b8d4e5b	2025-11-05	Warnings, Adverse reactions	Exact identifier ndc (product): 71335-2993

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
SW9M9BB5K3	PHENOBARBITAL SODIUM	57-30-7	PHENOBARBITAL SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312370	PHENobarbital 130 MG/ML Injectable Solution	PSN	94673663-cf49-42ad-a201-09195b8d4e5b	100
312370	phenobarbital 130 MG/ML Injectable Solution	SCD	94673663-cf49-42ad-a201-09195b8d4e5b	100

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
71335-2993-1	71335299301	25 VIAL in 1 BOX, UNIT-DOSE (71335-2993-1) / 1 mL in 1 VIAL (71335-2993-2)	25 vial	2025-11-05	No	No	Current
71335-2993-2	71335299302	1 mL in 1 VIAL	1 ml				Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Phenobarbital Sodium Injection, USP	Bryant Ranch Prepack	2025-11-05	HUMAN PRESCRIPTION DRUG LABEL	100