Etodolac
- Product NDC
- 63629-7128
- 11-digit product format
- 636297128
- Labeler code
- 63629
- Product ID
- 63629-7128_76071af4-cef5-4c6d-a224-6ff125a74a16
- 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
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7128-1 | 63629712801 | 30 TABLET, COATED in 1 BOTTLE (63629-7128-1) | 2016-11-03 | 0000-00-00 | No | No | Current |
| 63629-7128-2 | 63629712802 | 60 TABLET, COATED in 1 BOTTLE (63629-7128-2) | 2016-11-03 | 0000-00-00 | No | No | Current |