NDC codes

FDA NDC Directory
Product NDC (as listed)0143-1500Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-1500Add 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
0143-1500-010014315000100143150001100 TABLET in 1 BOTTLE (0143-1500-01)Marketed from Mar 5, 2020
0143-1500-050014315000500143150005500 TABLET in 1 BOTTLE (0143-1500-05)Marketed from Mar 5, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 30 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Hikma Pharmaceuticals USA Inc.NDC labeler code 0143
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
DEA schedule
CIV
Identifiers
Product ID 0143-1500_3ccf4b4a-2458-4ea0-8feb-8f3ff9980bb5SPL ID 3ccf4b4a-2458-4ea0-8feb-8f3ff9980bb5SPL set ID 8f02e85a-6dca-467d-b2bf-ab2f9fa9ef3bRxCUI 198083, 198089, 312357, 312362UNII 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

N400143150001 followed by a unit qualifier and the quantity

Package 00143-1500-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 0143-1500

What is NDC 0143-1500?
0143-1500 is the product NDC for Phenobarbital, Phenobarbital 30 mg/1 tablet, listed with the FDA by Hikma Pharmaceuticals USA Inc.. It has 2 package NDCs, 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?
Hikma Pharmaceuticals USA Inc., NDC labeler code 0143. 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?
153 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 32.4 mg/1TabletOralChartwell RX, LLC62135-55462135-0554-90
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralChartwell RX, LLC62135-55762135-0557-90
PhenobarbitalPhenobarbital 97.2 mg/1TabletOralChartwell RX, LLC62135-55862135-0558-90
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralREMEDYREPACK INC.70518-471770518-4717-00
PhenobarbitalPhenobarbital 32.4 mg/1TabletOralREMEDYREPACK INC.70518-471870518-4718-00

All 154 Phenobarbital NDCs

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