Fenoprofen calcium
- Product NDC
- 71993-313
- 11-digit product format
- 719930313
- Labeler code
- 71993
- Product ID
- 71993-313_51ac5c0c-2aef-abe1-e063-6294a90a7943
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenoprofen calcium
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Atland Pharmaceuticals, LLC
- Application
- ANDA214475
- Marketing category
- ANDA
- Marketing start
- 2026-05-15
- Substance
- FENOPROFEN CALCIUM
- Active strength
- 200 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fenoprofen calcium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FENOPROFEN CALCIUM | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0X2CW1QABJ |
| Rxcui | 197694 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71993-313-10 | Fenoprofen calcium | 100 in 1 BOTTLE | CAPSULE | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71993-313-10 | 71993031310 | 100 CAPSULE in 1 BOTTLE (71993-313-10) | 100 capsule | 2026-05-15 | No | No | Current |