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
- 85534-0019_5521c499-c95b-2cee-e063-6394a90aaf0a
- Product NDC
- 85534-0019
- Form
- TABLET
- Composition / generic term
- meloxicam
- Labeler
- HAWAII REPACK, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070307
- 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 (85534-0019-0) · 85534-0019-0
- 60 TABLET in 1 BOTTLE (85534-0019-1) · 85534-0019-1
- 90 TABLET in 1 BOTTLE (85534-0019-2) · 85534-0019-2
- 120 TABLET in 1 BOTTLE (85534-0019-3) · 85534-0019-3
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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