meloxicam
- Product NDC
- 50090-7495
- 11-digit product format
- 500907495
- Labeler code
- 50090
- Product ID
- 50090-7495_80c6d118-7003-4b1f-8528-9f64a9d81ca6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077921
- Marketing category
- ANDA
- Marketing start
- 2006-07-19
- Substance
- MELOXICAM
- Active strength
- 7.5 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VG2QF83CGL | MELOXICAM | 71125-38-7 | MELOXICAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7495-0 | 50090749500 | 90 TABLET in 1 BOTTLE (50090-7495-0) | 90 tablet | 2025-01-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| meloxicam | A-S Medication Solutions | 2025-02-11 | HUMAN PRESCRIPTION DRUG LABEL | 2 |