Etodolac
- Product NDC
- 55700-057
- 11-digit product format
- 557000057
- Labeler code
- 55700
- Product ID
- 55700-057_ae91bcbd-a2d3-4e6c-8696-3d449fd10bb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075074
- Marketing category
- ANDA
- Marketing start
- 2000-04-25
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],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 |