Meloxicam
- Product NDC
- 71335-3056
- 11-digit product format
- 713353056
- Labeler code
- 71335
- Product ID
- 71335-3056_3f28bdc5-a666-43a1-b8e2-06860012746e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077882
- Marketing category
- ANDA
- Marketing start
- 2025-10-20
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Meloxicam
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MELOXICAM | 7.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VG2QF83CGL |
| Rxcui | 311486 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-3056-1 | Meloxicam | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
| 71335-3056-2 | Meloxicam | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 71335-3056-3 | Meloxicam | 30 in 1 BOTTLE | TABLET | 30 | | 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 |
|---|
| 71335-3056-1 | 71335305601 | 500 TABLET in 1 BOTTLE (71335-3056-1) | 500 tablet | 2026-02-05 | No | No | Historical |
| 71335-3056-2 | 71335305602 | 60 TABLET in 1 BOTTLE (71335-3056-2) | 60 tablet | 2026-02-05 | No | No | Historical |
| 71335-3056-3 | 71335305603 | 30 TABLET in 1 BOTTLE (71335-3056-3) | 30 tablet | 2026-02-05 | No | No | Historical |