Etodolac
- Product NDC
- 71610-859
- 11-digit product format
- 716100859
- Labeler code
- 71610
- Product ID
- 71610-859_24259c72-b825-d77b-e063-6394a90ab496
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075074
- Marketing category
- ANDA
- Marketing start
- 1998-03-11
- Substance
- ETODOLAC
- Active strength
- 400 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2M36281008 | ETODOLAC | 41340-25-4 | ETODOLAC |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-859-30 | 71610085930 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-859-30) | 2024-10-10 | No | No | Historical |
| 71610-859-53 | 71610085953 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-859-53) | 2024-10-10 | No | No | Historical |
| 71610-859-60 | 71610085960 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-859-60) | 2024-10-10 | No | No | Historical |
| 71610-859-80 | 71610085980 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-859-80) | 2024-10-10 | No | No | Historical |