NDC codes

FDA NDC Directory
Product NDC (as listed)50090-2140Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-2140Add 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
50090-2140-05009021400030 TABLET, FILM COATED in 1 BOTTLE (50090-2140-0)Marketed from Oct 19, 2015
50090-2140-15009021400190 TABLET, FILM COATED in 1 BOTTLE (50090-2140-1)Marketed from Oct 19, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076921
Marketing start
Listing expires
Identifiers
Product ID 50090-2140_85874a9e-c3aa-4d72-9883-cf102d0190d4SPL ID 85874a9e-c3aa-4d72-9883-cf102d0190d4

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

N450090214000 followed by a unit qualifier and the quantity

Package 50090-2140-00. 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 50090-2140

What is NDC 50090-2140?
50090-2140 is the product NDC for Mirtazapine, Mirtazapine 15 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. 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?
A-S Medication Solutions, NDC labeler code 50090. 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 coatedOralANI Pharmaceuticals, Inc.70954-83070954-0830-10
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-866300615-8663-0500615-8663-39
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralCoupler LLC67046-048467046-0484-03
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralCoupler LLC67046-006867046-0068-03
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralSafecor Health LLC48433-07648433-0076-20
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralSafecor Health LLC48433-07748433-0077-20

All 139 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
ProductStrengthForm · routeLabelerProduct NDC
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2635
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-3038
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4989
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0180
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8489
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-2800
MirtazapineMirtazapine 7.5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2819
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2784
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1332
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8459
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-119
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralCoupler LLC67046-2024
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-120
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-121
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralDirect_Rx72189-626
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralCoupler LLC67046-0068
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-3346
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0305
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCoupler LLC67046-0319
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0964

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