What is NDC 68462-881?

68462-881 is the product NDC for Tacrolimus, Tacrolimus .3 mg/g ointment, listed with the FDA by Glenmark Pharmaceuticals Inc., USA. It has 3 package NDCs, shown above in 10- and 11-digit form.

Glenmark Pharmaceuticals Inc., USA, NDC labeler code 68462. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tacrolimus?

93 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tacrolimus NDC 68462-881 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68462-881Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68462-0881Add 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
68462-881-35	6846208813568462088135	1 TUBE in 1 CARTON (68462-881-35) / 30 g in 1 TUBEMarketed from Aug 16, 2023
68462-881-65	6846208816568462088165	1 TUBE in 1 CARTON (68462-881-65) / 60 g in 1 TUBEMarketed from Aug 16, 2023
68462-881-94	6846208819468462088194	1 TUBE in 1 CARTON (68462-881-94) / 100 g in 1 TUBEMarketed from Aug 16, 2023

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): Tacrolimus
Generic name (nonproprietary): tacrolimus
Active ingredients: Tacrolimus — .3 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Glenmark Pharmaceuticals Inc., USANDC labeler code 68462
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210393
Marketing start: Aug 16, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Calcineurin Inhibitors (Mechanism)
Identifiers: Product ID 68462-881_15dcd504-ee3e-4f0f-a765-55e31511641eSPL ID 15dcd504-ee3e-4f0f-a765-55e31511641eSPL set ID c2d2e3a1-f346-4245-b445-6dd44e371180RxCUI 313189, 314266UNII WM0HAQ4WNMUPC 0368462534946, 0368462881941
Pharmacologic class: Calcineurin Inhibitor Immunosuppressant

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468462088135 followed by a unit qualifier and the quantity

Package 68462-0881-35. 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 Apr 15, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Tacrolimus ointment, both 0.03% and 0.1% for adults, and only 0.03% for children aged 2 to 15 years, is indicated as second-line therapy for the short-term and non-continuous chronic treatment of moderate to severe atopic dermatitis in non-immunocompromised adults and children who have failed to respond adequately to other topical prescription treatments for atopic dermatitis, or when those treatments are not advisable. Tacrolimus ointment is not indicated for children younger than 2 years of age (see boxed WARNING, WARNINGS and PRECAUTIONS: Pediatric Use).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68462-881

What is NDC 68462-881?: 68462-881 is the product NDC for Tacrolimus, Tacrolimus .3 mg/g ointment, listed with the FDA by Glenmark Pharmaceuticals Inc., USA. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tacrolimus.
What is the active ingredient?: Tacrolimus.
Who is the labeler?: Glenmark Pharmaceuticals Inc., USA, NDC labeler code 68462. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tacrolimus?: 93 other product NDCs are listed under this name. See all Tacrolimus 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 Tacrolimus NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tacrolimus	Tacrolimus .5 mg/1	CapsuleOral	AvPAK	50268-736	50268-0736-15
Tacrolimus	Tacrolimus 1 mg/1	CapsuleOral	AvPAK	50268-737	50268-0737-15
Tacrolimus	Tacrolimus .5 mg/1	CapsuleOral	Safecor Health LLC	48433-092	48433-0092-20
Tacrolimus	Tacrolimus 1 mg/1	CapsuleOral	Safecor Health LLC	48433-093	48433-0093-20
Tacrolimus	Tacrolimus 5 mg/1	CapsuleOral	Safecor Health LLC	48433-094	48433-0094-20
Tacrolimus	Tacrolimus .5 mg/1	Capsule, Extended releaseOral	Amneal Pharmaceuticals NY LLC	69238-2780	69238-2780-03
Tacrolimus	Tacrolimus 1 mg/1	Capsule, Extended releaseOral	Amneal Pharmaceuticals NY LLC	69238-2781	69238-2781-03
Tacrolimus	Tacrolimus 5 mg/1	Capsule, Extended releaseOral	Amneal Pharmaceuticals NY LLC	69238-2782	69238-2782-03
Tacrolimus	Tacrolimus 5 mg/mL	InjectionIntravenous	Nexus Pharmaceuticals, LLC	14789-135	14789-0135-05
Tacrolimus	Tacrolimus .5 mg/1	CapsuleOral	Stellon Biotech Inc.	85972-101	85972-0101-0185972-0101-30

All 94 Tacrolimus NDCs

Other NDCs under ANDA 210393

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

FDA NDC Directory listings under ANDA 210393
Product	Strength	Form · route	Labeler	Product NDC
Tacrolimus	Tacrolimus 1 mg/g	OintmentTopical	Glenmark Pharmaceuticals Inc., USA	68462-534