Etodolac
- Product NDC
- 60429-315
- 11-digit product format
- 604290315
- Labeler code
- 60429
- Product ID
- 60429-315_e6d9606c-ac46-b89c-e053-2995a90ac780
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076174
- Marketing category
- ANDA
- Marketing start
- 2003-03-13
- Marketing end
- 2024-01-31
- Substance
- ETODOLAC
- Active strength
- 600 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
- 0000-00-00
- 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 |
|---|
| 60429-315-01 | 60429031501 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-315-01) | 2011-07-18 | 0000-00-00 | No | No | Current |