NDC codes

FDA NDC Directory
Product NDC (as listed)71610-881Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0881Add 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
71610-881-307161008813030 TABLET in 1 BOTTLE (71610-881-30)Marketed from Feb 20, 2025

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 — 7.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077920
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 71610-881_2eaaaae3-9819-9201-e063-6394a90a94c3SPL ID 2eaaaae3-9819-9201-e063-6394a90a94c3SPL set ID 2eaac8b2-d50a-a0bc-e063-6294a90a7cacRxCUI 311486UNII 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

N471610088130 followed by a unit qualifier and the quantity

Package 71610-0881-30. 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. INDICATIONS AND USAGE 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 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 poly…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077920

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

FDA NDC Directory listings under ANDA 077920
ProductStrengthForm · routeLabelerProduct NDC
MeloxicamMeloxicam 15 mg/1TabletOralAiPing Pharmaceutical, Inc11788-099
MeloxicamMeloxicam 7.5 mg/1TabletOralAiPing Pharmaceutical, Inc11788-098
MeloxicamMeloxicam 15 mg/1TabletOralMedcore LLC82461-712
MeloxicamMeloxicam 7.5 mg/1TabletOralMedcore LLC82461-719
MeloxicamMeloxicam 15 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-872
MeloxicamMeloxicam 15 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-403
MeloxicamMeloxicam 7.5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-402
MeloxicamMeloxicam 7.5 mg/1TabletOralAiPing Pharmaceutical, Inc11788-046
MeloxicamMeloxicam 15 mg/1TabletOralAiPing Pharmaceutical, Inc11788-047
MeloxicamMeloxicam 15 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-447
MeloxicamMeloxicam 7.5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-446
MeloxicamMeloxicam 15 mg/1TabletOralChartwell RX, LLC62135-716
MeloxicamMeloxicam 7.5 mg/1TabletOralChartwell RX, LLC62135-715

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