Flurbiprofen
- Product NDC
- 63629-8808
- 11-digit product format
- 636298808
- Labeler code
- 63629
- Product ID
- 63629-8808_a91f60d1-facf-428e-8c1a-d57008beada4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurbiprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074431
- Marketing category
- ANDA
- Marketing start
- 1995-06-02
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Flurbiprofen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLURBIPROFEN | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5GRO578KLP |
| Rxcui | 197724 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-8808-1 | Flurbiprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8808 | FLURBIPROFEN TABLET, FILM COATED [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 1 package rows | 20240113_745337de-5378-4f1d-b457-d2f45f2df665.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 |
|---|
| 63629-8808-1 | 63629880801 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-8808-1) | 1995-06-02 | 0000-00-00 | No | No | Current |