MELOXICAM
- Product NDC
- 82804-029
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077929
- Marketing category
- ANDA
- Substance
- MELOXICAM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 82804-029-30 | 30 TABLET in 1 BOTTLE (82804-029-30) | 2023-12-18 | | No | Historical |
| 82804-029-60 | 60 TABLET in 1 BOTTLE (82804-029-60) | 2023-12-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| MELOXICAM | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |