Etodolac
- Product NDC
- 50090-1316
- 11-digit product format
- 500901316
- Labeler code
- 50090
- Product ID
- 50090-1316_d8755afb-5caa-4f61-b021-a718d13f1f8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076174
- Marketing category
- ANDA
- Marketing start
- 2003-03-13
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 600 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2M36281008 | ETODOLAC | 41340-25-4 | ETODOLAC |