Meloxicam
- Product NDC
- 67296-1250
- 11-digit product format
- 672961250
- Labeler code
- 67296
- Product ID
- 67296-1250_d6102263-b02c-015c-e053-2995a90a5370
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA078008
- Marketing category
- ANDA
- Marketing start
- 2006-10-02
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1250-2 | Meloxicam | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1250 | MELOXICAM TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20220121_525711af-c858-28bf-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1250-2 | 67296125002 | 20 TABLET in 1 BOTTLE (67296-1250-2) | 20 tablet | 2006-10-02 | 0000-00-00 | No | No | Current |