Meloxicam
- Product NDC
- 71740-339
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meloxicam
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Avondale Pharmaceuticals, LLC
- Application
- NDA021530
- Marketing category
- NDA
- Substance
- MELOXICAM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71740-339-11 | 1 BOTTLE, PLASTIC in 1 CARTON (71740-339-11) / 100 mL in 1 BOTTLE, PLASTIC | 20220621 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 4ddf5a4d-8e84-419d-8e3a-c91b85501885 | These highlights do not include all the information needed to use meloxicam oral suspension safely and effectively. See full prescribing information for meloxicam oral suspension. Meloxicam oral suspension Initial U.S. Approval: 2004 | Avondale Pharmaceuticals, LLC | 2024-01-24 | HUMAN PRESCRIPTION DRUG LABEL | 2 |