Etodolac
- Product NDC
- 63187-796
- 11-digit product format
- 631870796
- Labeler code
- 63187
- Product ID
- 63187-796_4ad5fa04-03c3-4a42-abc3-781f435387e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075009
- Marketing category
- ANDA
- Marketing start
- 1998-05-20
- 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
- 2020-12-31
- 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 |
|---|
| 63187-796-20 | 63187079620 | 20 TABLET, FILM COATED in 1 BOTTLE (63187-796-20) | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-796-30 | 63187079630 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-796-30) | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-796-60 | 63187079660 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-796-60) | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-796-90 | 63187079690 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-796-90) | 2016-12-01 | 0000-00-00 | No | No | Current |