SULINDAC
- Product NDC
- 71335-0535
- 11-digit product format
- 713350535
- Labeler code
- 71335
- Product ID
- 71335-0535_8638d33f-5a3a-49be-9bf1-a184422095db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SULINDAC
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072711
- Marketing category
- ANDA
- Marketing start
- 2010-01-25
- Marketing end
- 0000-00-00
- Substance
- SULINDAC
- 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 |
|---|
| 71335-0535-1 | 71335053501 | 30 TABLET in 1 BOTTLE (71335-0535-1) | 30 tablet | 2013-01-15 | 0000-00-00 | No | No | Current |
| 71335-0535-2 | 71335053502 | 60 TABLET in 1 BOTTLE (71335-0535-2) | 60 tablet | 2013-01-15 | 0000-00-00 | No | No | Current |
| 71335-0535-3 | 71335053503 | 20 TABLET in 1 BOTTLE (71335-0535-3) | 20 tablet | 2013-01-15 | 0000-00-00 | No | No | Current |
| 71335-0535-4 | 71335053504 | 14 TABLET in 1 BOTTLE (71335-0535-4) | 14 tablet | 2013-01-15 | 0000-00-00 | No | No | Current |
| 71335-0535-5 | 71335053505 | 90 TABLET in 1 BOTTLE (71335-0535-5) | 90 tablet | 2013-01-15 | 0000-00-00 | No | No | Current |