Flurbiprofen
- Product NDC
- 68788-7341
- 11-digit product format
- 687887341
- Labeler code
- 68788
- Product ID
- 68788-7341_aed7f70b-f642-4b53-959c-90e0a675d541
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074431
- Marketing category
- ANDA
- Marketing start
- 2019-03-08
- Marketing end
- 0000-00-00
- Substance
- FLURBIPROFEN
- Active strength
- 100 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7341 | FLURBIPROFEN TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.] | 7 | Legacy NDC | 20240502_a0e9620d-0951-44d7-af6c-9b642051bd74.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7341-1 | 68788734101 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7341-1) | 2019-03-08 | 0000-00-00 | No | No | Current |
| 68788-7341-3 | 68788734103 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7341-3) | 2019-03-08 | 0000-00-00 | No | No | Current |
| 68788-7341-6 | 68788734106 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7341-6) | 2019-03-08 | 0000-00-00 | No | No | Current |
| 68788-7341-9 | 68788734109 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7341-9) | 2019-03-08 | 0000-00-00 | No | No | Current |