Etodolac
- Product NDC
- 71335-0092
- 11-digit product format
- 713350092
- Labeler code
- 71335
- Product ID
- 71335-0092_0357a5ce-1b34-4cbb-a171-44ea756aab7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075009
- Marketing category
- ANDA
- Marketing start
- 2009-09-09
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 500 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
- 2021-12-31
- 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 |
|---|
| 71335-0092-1 | 71335009201 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0092-1) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-2 | 71335009202 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0092-2) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-3 | 71335009203 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0092-3) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-4 | 71335009204 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0092-4) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-5 | 71335009205 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-0092-5) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-6 | 71335009206 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0092-6) | 2011-09-12 | 0000-00-00 | No | No | Current |
| 71335-0092-7 | 71335009207 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0092-7) | 2011-09-12 | 0000-00-00 | No | No | Current |