What is NDC 57237-008?

57237-008 is the product NDC for Mirtazapine, Mirtazapine 15 mg/1 tablet, film coated, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Rising Pharma Holdings, Inc., NDC labeler code 57237. 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?

133 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 57237-008 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)57237-008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57237-0008Add 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
57237-008-05	57237000805	500 TABLET, FILM COATED in 1 BOTTLE (57237-008-05)Marketed from Oct 22, 2004
57237-008-30	57237000830	30 TABLET, FILM COATED in 1 BOTTLE (57237-008-30)Marketed from Oct 22, 2004

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: Rising Pharma Holdings, Inc.NDC labeler code 57237
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076921
Marketing start: Oct 22, 2004
Listing expires: Dec 31, 2026
Identifiers: Product ID 57237-008_7616f3f3-c42e-474d-b201-0235120cff36SPL ID 7616f3f3-c42e-474d-b201-0235120cff36SPL set ID 58e9b4c6-531f-49c4-a640-6953e70892feRxCUI 311725, 311726, 314111, 476809UNII A051Q2099QUPC 0357237007303

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

N457237000805 followed by a unit qualifier and the quantity

Package 57237-0008-05. 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

Current FDA label (SPL), effective Sep 12, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Mirtazapine tablets are indicated for the treatment of major depressive disorder (MDD) in adults [see Clinical Studies (14) ]. Mirtazapine tablets are indicated for the treatment of major depressive disorder (MDD) in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 57237-008

What is NDC 57237-008?: 57237-008 is the product NDC for Mirtazapine, Mirtazapine 15 mg/1 tablet, film coated, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 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?: Rising Pharma Holdings, Inc., NDC labeler code 57237. 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?: 133 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 15 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-076	48433-0076-20
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-077	48433-0077-20

All 134 Mirtazapine NDCs

Other NDCs under ANDA 076921

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

FDA NDC Directory listings under ANDA 076921
Product	Strength	Form · route	Labeler	Product NDC
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, Inc dba Vangard Labs	0615-8268
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, Inc dba Vangard Labs	0615-8269
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8489
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	Aurolife Pharma LLC	13107-001
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Aurolife Pharma LLC	13107-003
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Aurolife Pharma LLC	13107-031
Mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	Aurolife Pharma LLC	13107-032
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	ATLANTIC BIOLOGICALS CORP.	17856-0101
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2140
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2558
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2800
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	57237-007
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	57237-009
Mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	57237-010
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-584
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-403
Mirtazapine	Mirtazapine 45 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-3346
Mirtazapine	Mirtazapine 7.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-9255
Mirtazapine	Mirtazapine 30 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0068
Mirtazapine	Mirtazapine 15 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0319

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