Flurbiprofen
- Product NDC
- 68071-2480
- 11-digit product format
- 680712480
- Labeler code
- 68071
- Product ID
- 68071-2480_c790fbcf-b5d8-a148-e053-2a95a90a2840
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA074431
- Marketing category
- ANDA
- Marketing start
- 1995-06-02
- Marketing end
- 0000-00-00
- Substance
- FLURBIPROFEN
- Active strength
- 100 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2480-3 | Flurbiprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 68071-2480-4 | Flurbiprofen | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2480 | FLURBIPROFEN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 2 package rows | 20210721_c7911338-4071-f1d2-e053-2995a90a903d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2480-3 | 68071248003 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2480-3) | 2021-07-20 | 0000-00-00 | No | No | Current |
| 68071-2480-4 | 68071248004 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-2480-4) | 2021-07-20 | 0000-00-00 | No | No | Current |