What is NDC 72865-369?

72865-369 is the product NDC for mirtazapine, Mirtazapine 15 mg/1 tablet, film coated, listed with the FDA by XLCare Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

XLCare Pharmaceuticals Inc., NDC labeler code 72865. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for mirtazapine?

138 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

mirtazapine NDC 72865-369 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72865-369Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72865-0369Add 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
72865-369-05	7286503690572865036905	500 TABLET, FILM COATED in 1 BOTTLE (72865-369-05)Marketed from Oct 2, 2025
72865-369-10	7286503691072865036910	1000 TABLET, FILM COATED in 1 BOTTLE (72865-369-10)Marketed from Oct 2, 2025
72865-369-30	7286503693072865036930	30 TABLET, FILM COATED in 1 BOTTLE (72865-369-30)Marketed from Oct 2, 2025

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): mirtazapine
Generic name (nonproprietary): mirtazapine
Active ingredients: Mirtazapine — 15 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: XLCare Pharmaceuticals Inc.NDC labeler code 72865
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219721
Marketing start: Oct 2, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 72865-369_5cc67a1a-2e3d-3916-e063-6294a90a1ecaSPL ID 5cc67a1a-2e3d-3916-e063-6294a90a1eca

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

N472865036905 followed by a unit qualifier and the quantity

Package 72865-0369-05. 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 72865-369

What is NDC 72865-369?: 72865-369 is the product NDC for mirtazapine, Mirtazapine 15 mg/1 tablet, film coated, listed with the FDA by XLCare Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: mirtazapine.
What is the active ingredient?: Mirtazapine.
Who is the labeler?: XLCare Pharmaceuticals Inc., NDC labeler code 72865. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for mirtazapine?: 138 other product NDCs are listed under this name. See all mirtazapine 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 mirtazapine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0319	67046-0319-03
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0280	55154-0280-00
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0625	67046-0625-03
Mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-2024	67046-2024-03
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8663	00615-8663-0500615-8663-39
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	ANI Pharmaceuticals, Inc.	70954-830	70954-0830-10
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0484	67046-0484-03
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0068	67046-0068-03
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-077	48433-0077-20
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-076	48433-0076-20

All 139 mirtazapine NDCs

Other NDCs under ANDA 219721

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

FDA NDC Directory listings under ANDA 219721
Product	Strength	Form · route	Labeler	Product NDC
mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-407
mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-408
mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-409
mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-410
mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8019
mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	XLCare Pharmaceuticals Inc.	72865-368
mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	XLCare Pharmaceuticals Inc.	72865-370
mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	XLCare Pharmaceuticals Inc.	72865-371