Celecoxib
- Product NDC
- 60760-849
- 11-digit product format
- 607600849
- Labeler code
- 60760
- Product ID
- 60760-849_9c56c645-a24f-c288-e053-2a95a90ac603
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA204197
- Marketing category
- ANDA
- Marketing start
- 2015-06-03
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-849-15 | 60760084915 | 15 CAPSULE in 1 BOTTLE, PLASTIC (60760-849-15) | 15 capsule | 2017-11-14 | 0000-00-00 | No | No | Current |
| 60760-849-30 | 60760084930 | 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-849-30) | 30 capsule | 2017-11-14 | 0000-00-00 | No | No | Current |
| 60760-849-60 | 60760084960 | 60 CAPSULE in 1 BOTTLE, PLASTIC (60760-849-60) | 60 capsule | 2017-11-14 | 0000-00-00 | No | No | Current |