meloxicam
- Product NDC
- 63629-6706
- 11-digit product format
- 636296706
- Labeler code
- 63629
- Product ID
- 63629-6706_facee48f-e3ba-43e9-9a5f-99b11f8e2c5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077921
- Marketing category
- ANDA
- Marketing start
- 2006-07-19
- Marketing end
- 0000-00-00
- Substance
- MELOXICAM
- Active strength
- 15 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
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 |
|---|
| 63629-6706-1 | 63629670601 | 90 TABLET in 1 BOTTLE (63629-6706-1) | 90 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6706-2 | 63629670602 | 30 TABLET in 1 BOTTLE (63629-6706-2) | 30 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |