Sulindac
- Product NDC
- 0904-6216
- 11-digit product format
- 009046216
- Labeler code
- 0904
- Product ID
- 0904-6216_8f059053-2856-4abc-a23b-7e9bd780f637
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulindac
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA072711
- Marketing category
- ANDA
- Marketing start
- 2010-11-30
- Marketing end
- 0000-00-00
- Substance
- SULINDAC
- Active strength
- 150 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
- 2020-12-31
- 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 |
|---|
| 0904-6216-40 | 00904621640 | 500 TABLET in 1 BOTTLE (0904-6216-40) | 500 tablet | 2010-11-30 | 0000-00-00 | No | No | Current |