Etodolac
- Product NDC
- 50090-0591
- 11-digit product format
- 500900591
- Labeler code
- 50090
- Product ID
- 50090-0591_18f2bfde-8ec9-4e3d-9170-771cfa2bd0cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075074
- Marketing category
- ANDA
- Marketing start
- 1998-03-11
- 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
- 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 |