Etodolac
- Product NDC
- 55700-592
- 11-digit product format
- 557000592
- Labeler code
- 55700
- Product ID
- 55700-592_08e42176-f1fa-44cd-b285-8099d1ebf028
- 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
- 2018-04-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-592 | ETODOLAC TABLET, FILM COATED [QUALITY CARE PRODUCTS LLC] | 10 | Legacy NDC | 20241219_fb52802c-5161-4ca0-a7a6-9cebed639874.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-592-30 | 55700059230 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-592-30) | 2018-04-07 | 0000-00-00 | No | No | Current |
| 55700-592-60 | 55700059260 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-592-60) | 2018-04-07 | 0000-00-00 | No | No | Current |