Sulindac
- Product NDC
- 51079-667
- 11-digit product format
- 510790667
- Labeler code
- 51079
- Product ID
- 51079-667_9af1b4b7-ac35-2bc7-e053-2a95a90a6153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sulindac
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA073039
- Marketing category
- ANDA
- Marketing start
- 1997-02-04
- Marketing end
- 2021-03-31
- 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
- 0000-00-00
- 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 |
|---|
| 51079-667-20 | 51079066720 | 100 BLISTER PACK in 1 CARTON (51079-667-20) > 1 TABLET in 1 BLISTER PACK (51079-667-01) | 100 blister pack | 1997-02-04 | 2021-03-31 | No | No | Current |