meloxicam
- Product NDC
- 60760-404
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077927
- Marketing category
- ANDA
- Substance
- MELOXICAM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 60760-404-30 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-404-30) | 20160203 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 60c9ab35-4b6e-383d-e053-2a91aa0a26ad | These highlights do not include all the information needed to use Meloxicam Tablets USP. safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USP, for oral use Initial U.S. Approval: 2000 | St. Mary's Medical Park Pharmacy | 2025-12-08 | HUMAN PRESCRIPTION DRUG LABEL | 7 |