Meloxicam NDC 53225-3075

Product information

Brand name (proprietary)

Meloxicam

Generic name (nonproprietary)

meloxicam

Active ingredients

Meloxicam — 7.5 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Terrain Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077882

Marketing start

Oct 20, 2025

Listing expires

Dec 31, 2027

Other FDA classes

Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)

Identifiers

Product ID 53225-3075_5475fe8e-f544-b38a-e063-6394a90adbffSPL ID 5475fe8e-f544-b38a-e063-6394a90adbffSPL set ID b603255e-1fcf-42ec-ab62-9aa321cb7ac6RxCUI 152695, 311486UNII VG2QF83CGLUPC 0353225307523, 0353225301514, 0353225301576, 0353225301538, 0353225307516, 0353225307530, 0353225301545, 0353225307547, 0353225307554, 0353225301552, 0353225301521, 0353225301569, 0353225307578, 0353225307561

Pharmacologic class

Nonsteroidal Anti-inflammatory Drug

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

N453225307501 followed by a unit qualifier and the quantity Copy

Package 53225-3075-01. 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 077882

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