Etodolac
- Product NDC
- 55700-757
- 11-digit product format
- 557000757
- Labeler code
- 55700
- Product ID
- 55700-757_fd6bee29-d327-45c3-a5f8-160cd3d9eb27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA076004
- Marketing category
- ANDA
- Marketing start
- 2019-05-24
- 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 |
|---|
| 55700-757-30 | 55700075730 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-757-30) | 2019-05-24 | 0000-00-00 | No | No | Current |