NDC codes

FDA NDC Directory
Product NDC (as listed)63187-471Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0471Add 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
63187-471-306318704713030 TABLET, FILM COATED in 1 BOTTLE (63187-471-30)Marketed from Feb 2, 2015
63187-471-606318704716060 TABLET, FILM COATED in 1 BOTTLE (63187-471-60)Marketed from Feb 2, 2015
63187-471-906318704719090 TABLET, FILM COATED in 1 BOTTLE (63187-471-90)Marketed from Feb 2, 2015

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077666
Marketing start
Listing expires
Identifiers
Product ID 63187-471_fb4bf3e5-f62b-489a-ba75-8e94513f29caSPL ID fb4bf3e5-f62b-489a-ba75-8e94513f29caSPL set ID 3b516a33-b164-4e4f-bc18-e9d1e591323aRxCUI 311725, 311726UNII A051Q2099QUPC 0363187206307, 0363187471309

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

N463187047130 followed by a unit qualifier and the quantity

Package 63187-0471-30. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 077666

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

FDA NDC Directory listings under ANDA 077666
ProductStrengthForm · routeLabelerProduct NDC
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralProficient Rx LP63187-206
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralAvKARE42291-952
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralDirect_Rx61919-153
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC43353-378
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralMcKesson Corporation dba SKY Packaging63739-098
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralMcKesson Corporation dba SKY Packaging63739-099
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1058
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCoupler LLC67046-1590
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6519
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralApotex Corp.60505-0248
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralApotex Corp.60505-0247
MirtazapineMirtazapine 45 mg/1Tablet, Film coatedOralApotex Corp.60505-0249
MirtazapineMirtazapine 30 mg/1Tablet, Film coatedOralProficient Rx LP63187-554
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-717
MirtazapineMirtazapine 15 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7297

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