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
68788-7726_1e49911f-6a20-4ac6-9457-18cf9a4770ba
Product NDC
68788-7726
Form
TABLET
Composition / generic term
meloxicam
Labeler
Preferred Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200701
Source listing expiry
20271231

Source-listed ingredients

  • MELOXICAM — 7.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (68788-7726-0) · 68788-7726-0
  • 15 TABLET in 1 BOTTLE (68788-7726-1) · 68788-7726-1
  • 20 TABLET in 1 BOTTLE (68788-7726-2) · 68788-7726-2
  • 30 TABLET in 1 BOTTLE (68788-7726-3) · 68788-7726-3
  • 14 TABLET in 1 BOTTLE (68788-7726-4) · 68788-7726-4
  • 60 TABLET in 1 BOTTLE (68788-7726-6) · 68788-7726-6
  • 28 TABLET in 1 BOTTLE (68788-7726-8) · 68788-7726-8
  • 90 TABLET in 1 BOTTLE (68788-7726-9) · 68788-7726-9

Source and coverage

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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.

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