meloxicam
- Product NDC
- 68071-4987
- 11-digit product format
- 680714987
- Labeler code
- 68071
- Product ID
- 68071-4987_e845c388-28e4-2dd8-e053-2a95a90a8bfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077921
- Marketing category
- ANDA
- Marketing start
- 2006-07-19
- Marketing end
- 0000-00-00
- Substance
- MELOXICAM
- Active strength
- 8 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4987-3 | 68071498703 | 30 TABLET in 1 BOTTLE (68071-4987-3) | 30 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 68071-4987-5 | 68071498705 | 15 TABLET in 1 BOTTLE (68071-4987-5) | 15 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 68071-4987-6 | 68071498706 | 60 TABLET in 1 BOTTLE (68071-4987-6) | 60 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |