Etodolac
- Product NDC
- 71335-0602
- 11-digit product format
- 713350602
- Labeler code
- 71335
- Product ID
- 71335-0602_b77bc7a3-77b4-4f4b-92d0-c72e61ab7483
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074903
- Marketing category
- ANDA
- Marketing start
- 2015-04-20
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 400 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 |
|---|
| 71335-0602-1 | 71335060201 | 20 TABLET, COATED in 1 BOTTLE (71335-0602-1) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-2 | 71335060202 | 14 TABLET, COATED in 1 BOTTLE (71335-0602-2) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-3 | 71335060203 | 30 TABLET, COATED in 1 BOTTLE (71335-0602-3) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-4 | 71335060204 | 100 TABLET, COATED in 1 BOTTLE (71335-0602-4) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-5 | 71335060205 | 60 TABLET, COATED in 1 BOTTLE (71335-0602-5) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-6 | 71335060206 | 90 TABLET, COATED in 1 BOTTLE (71335-0602-6) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-7 | 71335060207 | 56 TABLET, COATED in 1 BOTTLE (71335-0602-7) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 71335-0602-8 | 71335060208 | 120 TABLET, COATED in 1 BOTTLE (71335-0602-8) | 2016-11-03 | 0000-00-00 | No | No | Current |