MELOXICAM
- Product NDC
- 72865-332
- 11-digit product format
- 728650332
- Labeler code
- 72865
- Product ID
- 72865-332_858d0bd6-67cd-4984-aa23-90d75b47596b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- XLCare Pharmaceuticals, Inc.
- Application
- ANDA217579
- Marketing category
- ANDA
- Marketing start
- 2025-12-12
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MELOXICAM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MELOXICAM | 7.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VG2QF83CGL |
| Rxcui | 152695, 311486 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72865-332-01 | MELOXICAM | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 72865-332-10 | MELOXICAM | 1000 in 1 BOTTLE | TABLET | 1000 | | 1 |
| 72865-332-90 | MELOXICAM | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72865-332-01 | 72865033201 | 100 TABLET in 1 BOTTLE (72865-332-01) | 100 tablet | 2025-12-12 | No | No | Current |
| 72865-332-10 | 72865033210 | 1000 TABLET in 1 BOTTLE (72865-332-10) | 1000 tablet | 2025-12-12 | No | No | Current |
| 72865-332-90 | 72865033290 | 90 TABLET in 1 BOTTLE (72865-332-90) | 90 tablet | 2025-12-12 | No | No | Current |