What is NDC 68083-136?

68083-136 is the product NDC for Heparin Sodium, Heparin sodium 5000 [USP'U]/mL injection, listed with the FDA by Gland Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Gland Pharma Limited, NDC labeler code 68083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Heparin Sodium?

108 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Heparin Sodium NDC 68083-136 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68083-136Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68083-0136Add 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 NDC	11-digit (billing)	Package	Copy
68083-136-25	68083013625	25 VIAL in 1 CARTON (68083-136-25) / 1 mL in 1 VIAL (68083-136-01)Marketed from Mar 9, 2017

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): Heparin Sodium
Generic name (nonproprietary): heparin sodium
Active ingredients: Heparin sodium — 5000 [USP'U]/mL
Dosage form: Injection
Route: Intravenous, Subcutaneous
Labeler: Gland Pharma LimitedNDC labeler code 68083
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205323
Marketing start: Mar 9, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Heparin (Chemical structure)
Identifiers: Product ID 68083-136_7b0f85d1-774a-4644-af2f-c798d9c202a2SPL ID 7b0f85d1-774a-4644-af2f-c798d9c202a2
Pharmacologic class: Anti-coagulant; Unfractionated 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

N468083013625 followed by a unit qualifier and the quantity

Package 68083-0136-25. 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 68083-136

What is NDC 68083-136?: 68083-136 is the product NDC for Heparin Sodium, Heparin sodium 5000 [USP'U]/mL injection, listed with the FDA by Gland Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Heparin Sodium.
What is the active ingredient?: Heparin sodium.
Who is the labeler?: Gland Pharma Limited, NDC labeler code 68083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Heparin Sodium?: 108 other product NDCs are listed under this name. See all Heparin 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 Heparin Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Heparin Sodium	Heparin sodium 5000 [USP'U]/.5mL	Injection, SolutionIntravenous, Subcutaneous	Cardinal Health 107, LLC	55154-9589	55154-9589-05
Heparin Sodium	Heparin sodium 5000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	REMEDYREPACK INC.	70518-4547	70518-4547-00
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Meitheal Pharmaceuticals Inc.	71288-449	71288-0449-02
Heparin Sodium	Heparin sodium 5000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Meitheal Pharmaceuticals Inc.	71288-450	71288-0450-02
Heparin Sodium	Heparin sodium 10000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Meitheal Pharmaceuticals Inc.	71288-451	71288-0451-02
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Medical Purchasing Solutions, LLC.	71872-7351	71872-7351-01
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Medical Purchasing Solutions, LLC	71872-7352	71872-7352-01
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	NorthStar RxLLC	72603-179	72603-0179-25
Heparin Sodium	Heparin sodium 5000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	NorthStar RxLLC	72603-214	72603-0214-25
Heparin Sodium	Heparin sodium 20000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	NorthStar RxLLC	72603-224	72603-0224-25

All 109 Heparin Sodium NDCs

Other NDCs under ANDA 205323

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

FDA NDC Directory listings under ANDA 205323
Product	Strength	Form · route	Labeler	Product NDC
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Gland Pharma Limited	68083-427
Heparin Sodium	Heparin sodium 1000 [USP'U]/mL	InjectionIntravenous, Subcutaneous	Gland Pharma Limited	68083-428