United States · FDA National Drug Code directory

Meloxicam

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
53225-3075_5475fe8e-f544-b38a-e063-6394a90adbff
Product NDC
53225-3075
Form
TABLET
Composition / generic term
Meloxicam
Labeler
Terrain Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20251020
Source listing expiry
20271231

Source-listed ingredients

  • MELOXICAM — 7.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (53225-3075-1) · 53225-3075-1
  • 60 TABLET in 1 BOTTLE (53225-3075-2) · 53225-3075-2
  • 90 TABLET in 1 BOTTLE (53225-3075-3) · 53225-3075-3
  • 100 TABLET in 1 BOTTLE (53225-3075-4) · 53225-3075-4
  • 120 TABLET in 1 BOTTLE (53225-3075-5) · 53225-3075-5
  • 500 TABLET in 1 BOTTLE (53225-3075-6) · 53225-3075-6
  • 1000 TABLET in 1 BOTTLE (53225-3075-7) · 53225-3075-7

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →