NDC codes

FDA NDC Directory
Product NDC (as listed)48433-078Labeler and product segments. Claims need a package NDC.
Product NDC at billing width48433-0078Add 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
48433-078-204843300782048433007820100 BLISTER PACK in 1 CARTON (48433-078-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-078-01)Marketed from Feb 5, 2026

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 — 45 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Safecor Health LLCNDC labeler code 48433
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076122
Marketing start
Listing expires
Identifiers
Product ID 48433-078_4c13278f-899f-f1b7-e063-6394a90ac5b7SPL ID 4c13278f-899f-f1b7-e063-6394a90ac5b7SPL set ID 6d2ff278-0c80-4373-b77d-b5f186c4b991RxCUI 311725, 311726, 314111UNII A051Q2099Q

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

N448433007820 followed by a unit qualifier and the quantity

Package 48433-0078-20. 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 . 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 48433-078

What is NDC 48433-078?
48433-078 is the product NDC for Mirtazapine, Mirtazapine 45 mg/1 tablet, film coated, listed with the FDA by Safecor Health LLC. It has 1 package NDC, 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?
Safecor Health LLC, NDC labeler code 48433. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCoupler LLC67046-031967046-0319-03
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-028055154-0280-00
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralCoupler LLC67046-062567046-0625-03
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralCoupler LLC67046-202467046-2024-03
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-866300615-8663-0500615-8663-39
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralANI Pharmaceuticals, Inc.70954-83070954-0830-10
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralCoupler LLC67046-048467046-0484-03
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralCoupler LLC67046-006867046-0068-03
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralSafecor Health LLC48433-07748433-0077-20
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralSafecor Health LLC48433-07648433-0076-20

All 139 Mirtazapine NDCs

Other NDCs under ANDA 076122

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

FDA NDC Directory listings under ANDA 076122
ProductStrengthForm · routeLabelerProduct NDC
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-475
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-3515
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-3530
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-523
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-3545
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralSafecor Health LLC48433-076
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4322
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralSafecor Health LLC48433-077
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-352
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-350
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-0280
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-351
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-5355
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-087
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-086
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-088

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