Etodolac
- Product NDC
- 50090-2133
- 11-digit product format
- 500902133
- Labeler code
- 50090
- Product ID
- 50090-2133_ec4e69ab-aa22-47ea-989f-f5d546dd113f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076004
- Marketing category
- ANDA
- Marketing start
- 2003-05-01
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 500 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2133-0 | 50090213300 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-2133-0) | 2015-10-15 | 0000-00-00 | No | No | Current |
| 50090-2133-5 | 50090213305 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-2133-5) | 2015-10-15 | 0000-00-00 | No | No | Current |