meloxicam
- Product NDC
- 63739-701
- 11-digit product format
- 637390701
- Labeler code
- 63739
- Product ID
- 63739-701_b3eb5a86-356f-74d4-e053-2a95a90abc58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meloxicam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077921
- Marketing category
- ANDA
- Marketing start
- 2006-07-19
- Marketing end
- 2021-08-21
- Substance
- MELOXICAM
- Active strength
- 8 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
- 0000-00-00
- 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 |
|---|
| 63739-701-10 | 63739070110 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-701-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2015-06-10 | 2021-08-21 | No | No | Current |