NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0585Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0585Add 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
80425-0585-18042505850130 TABLET in 1 BOTTLE (80425-0585-1)Marketed from Jun 18, 2026
80425-0585-28042505850260 TABLET in 1 BOTTLE (80425-0585-2)Marketed from Jun 18, 2026
80425-0585-38042505850390 TABLET in 1 BOTTLE (80425-0585-3)Marketed from Jun 18, 2026

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)
Meloxicam
Generic name (nonproprietary)
meloxicam
Active ingredients
Meloxicam — 15 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077882
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 80425-0585_57126403-c27a-e7d2-e063-6294a90abea6SPL ID 57126403-c27a-e7d2-e063-6294a90abea6SPL set ID 548ec3b7-2b6d-cd9e-e063-6394a90a78ffRxCUI 152695UNII VG2QF83CGL

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

N480425058501 followed by a unit qualifier and the quantity

Package 80425-0585-01. 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

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

Indications (excerpt from the label)

<p>Meloxicam tablets are a non-steroidal anti-inflammatory drug indicated for:</p> <ul> <li>Osteoarthritis (OA) ( <a href="#Section_1.1">1.1</a>)</li> <li>Rheumatoid Arthritis (RA) ( <a href="#Section_1.2">1.2</a>)</li> <li>Juvenile Rheumatoid Arthritis (JRA) in patients who weigh ≥60 kg ( <a href="#Section_1.3">1.3</a>)</li> </ul> Meloxicam tablets are a non-steroidal anti-inflammatory drug indicated for: Osteoarthritis (OA) ( 1.1 ) Rheumatoid Arthritis (RA) ( 1.2 ) Juvenile Rheumatoid Arthritis (JRA) in patients who weigh ≥60 kg ( 1.3 ) 1.1 Osteoarthritis (OA) Meloxicam tablets are indicated for relief of the signs and symptoms of osteoarthritis [see Clinical Studies (14.1) ] . 1.2 Rheumat…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077882

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

FDA NDC Directory listings under ANDA 077882
ProductStrengthForm · routeLabelerProduct NDC
MeloxicamMeloxicam 7.5 mg/1TabletOralBryant Ranch Prepack71335-3056
MeloxicamMeloxicam 15 mg/1TabletOralTerrain Pharmaceuticals, Inc.53225-3015
MeloxicamMeloxicam 7.5 mg/1TabletOralTerrain Pharmaceuticals, Inc.53225-3075
MeloxicamMeloxicam 15 mg/1TabletOralDirect_Rx72189-684
MeloxicamMeloxicam 7.5 mg/1TabletOralDirect_Rx72189-683
MeloxicamMeloxicam 7.5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0558
MeloxicamMeloxicam 7.5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0563
MeloxicamMeloxicam 7.5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0559
MeloxicamMeloxicam 15 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0584
MeloxicamMeloxicam 15 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0586

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