MELOXICAM
- Product NDC
- 70934-476
- 11-digit product format
- 709340476
- Labeler code
- 70934
- Product ID
- 70934-476_a824e5cf-85f9-7abe-e053-2995a90a9b48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA077929
- Marketing category
- ANDA
- Marketing start
- 2020-01-02
- Marketing end
- 0000-00-00
- Substance
- MELOXICAM
- Active strength
- 8 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-476-60 | 70934047660 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-476-60) | 60 tablet | 2020-01-02 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| MELOXICAM | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-01-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |