NDC codes

FDA NDC Directory
Product NDC (as listed)72189-684Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0684Add 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
72189-684-307218906843030 TABLET in 1 BOTTLE (72189-684-30)Marketed from Aug 12, 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)
Meloxicam
Generic name (nonproprietary)
meloxicam
Active ingredients
Meloxicam — 15 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_Rx
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 72189-684_58dbce26-b2ad-2ce4-e063-6294a90a5727SPL ID 58dbce26-b2ad-2ce4-e063-6294a90a5727SPL set ID 58dbce26-b2ac-2ce4-e063-6294a90a5727RxCUI 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

N472189068430 followed by a unit qualifier and the quantity

Package 72189-0684-30. 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

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

Indications (excerpt from the label)

. 1.1 Osteoarthritis (OA) Meloxicam tablets are indicated for relief of the signs and symptoms of osteoarthritis [see Clinical Studies (14.1)] . 1.2 Rheumatoid Arthritis (RA) Meloxicam tablets are indicated for relief of the signs and symptoms of rheumatoid arthritis [see Clinical Studies (14.1)] . 1.3 Juvenile Rheumatoid Arthritis (JRA) Pauciarticular and Polyarticular Course Meloxicam tablets are indicated for relief of the signs and symptoms of pauciarticular or polyarticular course Juvenile Rheumatoid Arthritis in patients who weigh ≥60 kg [see Dosage and Administration (2.4)and Clinical Studies (14.2)] .

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 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, LLC80425-0585
MeloxicamMeloxicam 15 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0584
MeloxicamMeloxicam 15 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0586

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