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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0X2CW1QABJ | FENOPROFEN CALCIUM | 53746-45-5 | FENOPROFEN CALCIUM |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fenoprofen calcium | Atland Pharmaceuticals, LLC | 2026-05-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |