NDC codes

FDA NDC Directory
Product NDC (as listed)67046-1434Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-1434Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
67046-1434-36704614340330 TABLET in 1 BLISTER PACK (67046-1434-3)Marketed from Jul 2, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Phenobarbital
Generic name (nonproprietary)
phenobarbital
Active ingredients
Phenobarbital — 64.8 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Coupler LLCNDC labeler code 67046
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
DEA schedule
CIV
Identifiers
Product ID 67046-1434_38f737f8-385d-f2b6-e063-6394a90ac88dSPL ID 38f737f8-385d-f2b6-e063-6394a90ac88dSPL set ID 38f738a5-1c2f-b404-e063-6294a90a9879RxCUI 199168UNII YQE403BP4D

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N467046143403 followed by a unit qualifier and the quantity

Package 67046-1434-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Phenobarbital Tablets, USP are indicated for use as a sedative or anticonvulsant.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67046-1434

What is NDC 67046-1434?
67046-1434 is the product NDC for Phenobarbital, Phenobarbital 64.8 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phenobarbital.
What is the active ingredient?
Phenobarbital.
Who is the labeler?
Coupler LLC, NDC labeler code 67046. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phenobarbital?
157 other product NDCs are listed under this name. See all Phenobarbital NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Phenobarbital NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PhenobarbitalPhenobarbital 15 mg/1TabletOralChartwell RX, LLC62135-51062135-0510-90
PhenobarbitalPhenobarbital 30 mg/1TabletOralChartwell RX, LLC62135-51462135-0514-90
PhenobarbitalPhenobarbital 60 mg/1TabletOralChartwell RX, LLC62135-51562135-0515-90
PhenobarbitalPhenobarbital 100 mg/1TabletOralChartwell RX, LLC62135-51962135-0519-90
PhenobarbitalPhenobarbital 16.2 mg/1TabletOralChartwell RX, LLC62135-53962135-0539-90
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralChartwell RX, LLC62135-55762135-0557-90
PhenobarbitalPhenobarbital 32.4 mg/1TabletOralChartwell RX, LLC62135-55462135-0554-90
PhenobarbitalPhenobarbital 97.2 mg/1TabletOralChartwell RX, LLC62135-55862135-0558-90
PhenobarbitalPhenobarbital 32.4 mg/1TabletOralREMEDYREPACK INC.70518-471870518-4718-00
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralREMEDYREPACK INC.70518-471770518-4717-00

All 158 Phenobarbital NDCs

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