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
29300-124_781188ae-3eef-498f-9d44-24a611027d7e
Product NDC
29300-124
Form
TABLET
Composition / generic term
meloxicam
Labeler
Unichem Pharmaceuticals (USA), Inc.
Marketing category
ANDA
Marketing start / end (source format)
20070307
Source listing expiry
20261231

Source-listed ingredients

  • MELOXICAM — 7.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (29300-124-01) · 29300-124-01
  • 500 TABLET in 1 BOTTLE (29300-124-05) · 29300-124-05
  • 1000 TABLET in 1 BOTTLE (29300-124-10) · 29300-124-10
  • 30 TABLET in 1 BOTTLE (29300-124-13) · 29300-124-13
  • 90 TABLET in 1 BOTTLE (29300-124-19) · 29300-124-19
  • 5000 TABLET in 1 BOTTLE (29300-124-50) · 29300-124-50

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 →