Meloxicam
- Product NDC
- 69336-102
- 11-digit product format
- 693360102
- Labeler code
- 69336
- Product ID
- 69336-102_456848c7-5e8b-44ca-8f6d-8d1ecd6464f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- STERLING KNIGHT PHARMACEUTICALS, LLC
- Application
- ANDA077918
- Marketing category
- ANDA
- Marketing start
- 2010-06-30
- 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
- 2019-12-31
- 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 |
|---|
| 69336-102-30 | Meloxicam | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69336-102 | MELOXICAM TABLET [STERLING KNIGHT PHARMACEUTICALS, LLC] | 2 | Legacy NDC, 1 package rows | 20151230_39ef545b-3a0d-4a84-97da-885ed5f8b945.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69336-102-30 | 69336010230 | 30 in 1 BOTTLE, PLASTIC | Historical |