Etodolac
- Product NDC
- 70934-346
- 11-digit product format
- 709340346
- Labeler code
- 70934
- Product ID
- 70934-346_b7afde6f-9f5e-86ab-e053-2995a90aebc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074903
- Marketing category
- ANDA
- Marketing start
- 2019-04-23
- 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
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 |
|---|
| 70934-346-30 | 70934034630 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-346-30) | 2019-04-23 | 0000-00-00 | No | No | Current |