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
- 11788-046_4ab12c6b-d2bf-4200-95f3-62b2a6cd1e43
- Product NDC
- 11788-046
- Form
- TABLET
- Composition / generic term
- Meloxicam
- Labeler
- AiPing Pharmaceutical, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251215
- 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 (11788-046-01) · 11788-046-01
- 500 TABLET in 1 BOTTLE (11788-046-05) · 11788-046-05
- 1000 TABLET in 1 BOTTLE (11788-046-10) · 11788-046-10
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 →