SULINDAC
- Product NDC
- 55700-682
- 11-digit product format
- 557000682
- Labeler code
- 55700
- Product ID
- 55700-682_0ca97d06-9339-4609-8ac5-282a28546293
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SULINDAC
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA072711
- Marketing category
- ANDA
- Marketing start
- 2018-09-14
- 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
- 2020-12-31
- 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 |
|---|
| 55700-682-60 | 55700068260 | 60 TABLET in 1 BOTTLE (55700-682-60) | 60 tablet | 2018-09-14 | 0000-00-00 | No | No | Current |