meloxicam
- Product NDC
- 50436-1125
- 11-digit product format
- 504361125
- Labeler code
- 50436
- Product ID
- 50436-1125_4c6010ac-d771-4a19-98f5-130efee9b671
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077927
- Marketing category
- ANDA
- Marketing start
- 2007-03-07
- 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
- 2022-12-31
- 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 |
|---|
| 50436-1125-1 | meloxicam | 30 in 1 BOTTLE | TABLET | 30 | | 16 |
| 50436-1125-2 | meloxicam | 60 in 1 BOTTLE | TABLET | 60 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-1125 | MELOXICAM TABLET [UNIT DOSE SERVICES] | 16 | Legacy NDC, 2 package rows | 20210819_f772d409-e1b8-46f9-9886-14de3f031b82.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 |
|---|
| 50436-1125-1 | 50436112501 | 30 TABLET in 1 BOTTLE (50436-1125-1) | 30 tablet | 2021-08-18 | 0000-00-00 | No | No | Current |
| 50436-1125-2 | 50436112502 | 60 TABLET in 1 BOTTLE (50436-1125-2) | 60 tablet | 2021-08-18 | 0000-00-00 | No | No | Current |