NDC codes

FDA NDC Directory
Product NDC (as listed)0143-9859Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-9859Add 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
0143-9859-25001439859250014398592525 VIAL in 1 BOX (0143-9859-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9859-01)Marketed from Jan 10, 2008

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)
Ceftriaxone
Generic name (nonproprietary)
ceftriaxone
Active ingredients
Ceftriaxone sodium — 250 mg/1
Dosage form
Injection, Powder, For solution
Route
Intramuscular, Intravenous
Labeler
Hikma Pharmaceuticals USA Inc.NDC labeler code 0143
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065342
Marketing start
Listing expires
Other FDA classes
Cephalosporins (Chemical structure)
Identifiers
Product ID 0143-9859_1553de11-36df-4e7e-a450-025b8563dd11SPL ID 1553de11-36df-4e7e-a450-025b8563dd11
Pharmacologic class
Cephalosporin Antibacterial

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 codeMed-Code curated

J0696 — Injection, ceftriaxone sodium, per 250 mg

Billing unit: 250 mg. Units on the claim = dose given ÷ 250 mg.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400143985925 followed by a unit qualifier and the quantity

Package 00143-9859-25. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0143-9859

What is NDC 0143-9859?
0143-9859 is the product NDC for Ceftriaxone, Ceftriaxone sodium 250 mg/1 injection, powder, for solution, listed with the FDA by Hikma Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ceftriaxone.
What is the active ingredient?
Ceftriaxone sodium.
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 Ceftriaxone?
17 other product NDCs are listed under this name. See all Ceftriaxone NDCs.
Is there a related HCPCS / J-code?
Yes: J0696, Injection, ceftriaxone sodium, per 250 mg. See Billing references above.

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

Other Ceftriaxone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CeftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousCivica, Inc.72572-06172572-0061-25
CeftriaxoneCeftriaxone sodium 2 g/1Injection, Powder, For solutionIntramuscular, IntravenousCivica, Inc.72572-06272572-0062-25
CeftriaxoneCeftriaxone sodium 10 g/1Injection, Powder, For solutionIntravenousHikma Pharmaceuticals USA Inc.0143-967800143-9678-01
Ceftriaxoneceftriaxone sodiumCeftriaxone sodium 100 g/1Injection, Powder, For solutionIntravenousSamson Medical Technologies, LLC66288-610066288-6100-01
CeftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousFresenius Kabi USA, LLC63323-34663323-0346-10
ceftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousSagent Pharmaceuticals25021-10625021-0106-10
ceftriaxoneCeftriaxone sodium 2 g/1Injection, Powder, For solutionIntramuscular, IntravenousSagent Pharmaceuticals25021-10725021-0107-20
CeftriaxoneCeftriaxone sodium 500 mg/1Injection, Powder, For solutionIntramuscular, IntravenousWG Critical Care, LLC44567-70044567-0700-25
CeftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousWG Critical Care, LLC44567-70144567-0701-95
CeftriaxoneCeftriaxone sodium 2 g/1Injection, Powder, For solutionIntramuscular, IntravenousWG Critical Care, LLC44567-70244567-0702-95

All 18 Ceftriaxone NDCs

Other NDCs under ANDA 065342

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 065342
ProductStrengthForm · routeLabelerProduct NDC
CeftriaxoneCeftriaxone sodium 2 g/1Injection, Powder, For solutionIntramuscular, IntravenousHikma Pharmaceuticals USA Inc.0143-9856
CeftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousHikma Pharmaceuticals USA Inc.0143-9857
CeftriaxoneCeftriaxone sodium 500 mg/1Injection, Powder, For solutionIntramuscular, IntravenousHikma Pharmaceuticals USA Inc.0143-9858
CeftriaxoneCeftriaxone sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousCivica, Inc.72572-061
CeftriaxoneCeftriaxone sodium 2 g/1Injection, Powder, For solutionIntramuscular, IntravenousCivica, Inc.72572-062

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