Etodolac
- Product NDC
- 42291-404
- 11-digit product format
- 422910404
- Labeler code
- 42291
- Product ID
- 42291-404_d57cb601-da16-2ffd-e053-2995a90a3808
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA075419
- Marketing category
- ANDA
- Marketing start
- 2017-01-05
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- 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
- 2023-12-31
- 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 |
|---|
| 42291-404-01 | 42291040401 | 100 CAPSULE in 1 BOTTLE (42291-404-01) | 100 capsule | 2017-01-05 | 0000-00-00 | No | No | Current |