Etodolac
- Product NDC
- 68788-7068
- 11-digit product format
- 687887068
- Labeler code
- 68788
- Product ID
- 68788-7068_8fc266e0-a963-4554-969f-58684872a195
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074903
- Marketing category
- ANDA
- Marketing start
- 2018-01-03
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 400 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7068-1 | 68788706801 | 100 TABLET, COATED in 1 BOTTLE (68788-7068-1) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 68788-7068-2 | 68788706802 | 20 TABLET, COATED in 1 BOTTLE (68788-7068-2) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 68788-7068-3 | 68788706803 | 30 TABLET, COATED in 1 BOTTLE (68788-7068-3) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 68788-7068-6 | 68788706806 | 60 TABLET, COATED in 1 BOTTLE (68788-7068-6) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 68788-7068-9 | 68788706809 | 90 TABLET, COATED in 1 BOTTLE (68788-7068-9) | 2018-01-03 | 0000-00-00 | No | No | Current |