Phenobarbital

Product NDC: 70518-4129
Requested package NDC: 70518-4129-0
11-digit product format: 705184129
Labeler code: 70518
Product ID: 70518-4129_5a7eee75-4060-cb76-e063-6294a90a4d5c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phenobarbital
Dosage form: TABLET
Route: ORAL
Labeler: REMEDYREPACK INC.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2024-07-01
Substance: PHENOBARBITAL
Active strength: 32.4 mg/1
DEA schedule: CIV
NDC exclude flag: No
Listing certified through: 2027-12-31
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: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PHENOBARBITAL	32.4 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
199167	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
4e2910f2-173d-4b5c-aad3-44f4ab40d8cb	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
70518-4129-0	Phenobarbital	30 in 1 BLISTER PACK	TABLET	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-4129	PHENOBARBITAL TABLET [REMEDYREPACK INC.]	2	Current NDC, 1 package rows	20250424_4e2910f2-173d-4b5c-aad3-44f4ab40d8cb.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	REMEDYREPACK INC.	4e2910f2-173d-4b5c-aad3-44f4ab40d8cb	2026-09-02	Warnings, Adverse reactions	Exact identifier ndc (package): 70518-4129-0 ndc (product): 70518-4129 ndc11 (package): 70518412900

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
199167	PHENobarbital 32.4 MG Oral Tablet	PSN	4e2910f2-173d-4b5c-aad3-44f4ab40d8cb	3
199167	phenobarbital 32.4 MG Oral Tablet	SCD	4e2910f2-173d-4b5c-aad3-44f4ab40d8cb	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
70518-4129-0	70518412900	30 TABLET in 1 BLISTER PACK (70518-4129-0)	30 tablet	2024-07-01	No	No	Current