Etodolac
- Product NDC
- 60760-378
- 11-digit product format
- 607600378
- Labeler code
- 60760
- Product ID
- 60760-378_a6a941ce-2f8e-430e-e053-2a95a90ae53d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076174
- Marketing category
- ANDA
- Marketing start
- 2003-03-13
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 500 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
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-378-15 | 60760037815 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-378-15) | 2020-05-19 | 0000-00-00 | No | No | Current |