NDC codes

FDA NDC Directory
Product NDC (as listed)68001-458Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68001-0458Add 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
68001-458-42680010458426800104584210 SYRINGE in 1 CARTON (68001-458-42) / .4 mL in 1 SYRINGE (68001-458-43)Marketed from Oct 19, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Enoxaparin Sodium
Generic name (nonproprietary)
enoxaparin sodium
Active ingredients
Enoxaparin sodium — 100 mg/mL
Dosage form
Injection
Route
Subcutaneous
Labeler
BluePoint LaboratoriesNDC labeler code 68001
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076684
Marketing start
Marketing end
Other FDA classes
Low-Molecular-Weight (Chemical structure)
Identifiers
Product ID 68001-458_5da039b6-9a0e-9330-e063-6294a90a5c16SPL ID 5da039b6-9a0e-9330-e063-6294a90a5c16
Pharmacologic class
Low Molecular Weight Heparin

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

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

N468001045842 followed by a unit qualifier and the quantity

Package 68001-0458-42. 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 68001-458

What is NDC 68001-458?
68001-458 is the product NDC for Enoxaparin Sodium, Enoxaparin sodium 100 mg/mL injection, listed with the FDA by BluePoint Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Enoxaparin Sodium.
What is the active ingredient?
Enoxaparin sodium.
Who is the labeler?
BluePoint Laboratories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Enoxaparin Sodium?
140 other product NDCs are listed under this name. See all Enoxaparin Sodium 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 Enoxaparin Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
enoxaparin sodiumEnoxaparin sodium 150 mg/mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10728955-0107-10
enoxaparin sodiumEnoxaparin sodium 80 mg/.8mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10428955-0104-10
enoxaparin sodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10528955-0105-10
enoxaparin sodiumEnoxaparin sodium 120 mg/.8mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10628955-0106-10
enoxaparin sodiumEnoxaparin sodium 60 mg/.6mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10328955-0103-10
enoxaparin sodiumEnoxaparin sodium 30 mg/.3mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10128955-0101-10
enoxaparin sodiumEnoxaparin sodium 40 mg/.4mLInjectionSubcutaneousHebei Changshan Biochemical Pharmaceutical Co., Ltd.28955-10228955-0102-10
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousCivica, Inc.72572-28072572-0280-10
Enoxaparin SodiumEnoxaparin sodium 300 mg/3mLInjectionIntravenous, SubcutaneousBluePoint Laboratories68001-64168001-0641-41
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousBluePoint Laboratories68001-63368001-0633-42

All 141 Enoxaparin Sodium NDCs

Other NDCs under ANDA 076684

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

FDA NDC Directory listings under ANDA 076684
ProductStrengthForm · routeLabelerProduct NDC
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5601
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5602
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5603
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5604
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5605
Enoxaparin SodiumEnoxaparin sodium 150 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5606
Enoxaparin SodiumEnoxaparin sodium 150 mg/mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-5607
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousBluePoint Laboratories68001-457
Enoxaparin SodiumEnoxaparin sodium 100 mg/mLInjectionSubcutaneousBluePoint Laboratories68001-459

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