MELOXICAM
- Product NDC
- 50090-7875
- 11-digit product format
- 500907875
- Labeler code
- 50090
- Product ID
- 50090-7875_39e2727b-37f1-4fb2-81cf-872ec7dcf082
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077929
- 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
- 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 |
|---|
| 50090-7875-0 | 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 |
|---|
| 50090-7875-0 | 50090787500 | 90 TABLET in 1 BOTTLE (50090-7875-0) | 90 tablet | 2026-01-30 | No | No | Current |