Nalfon
- Product NDC
- 71335-1302
- 11-digit product format
- 713351302
- Labeler code
- 71335
- Product ID
- 71335-1302_e51d2975-e7ca-4c2a-b530-b96686e104f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenoprofen calcium
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA017604
- Marketing category
- NDA
- Marketing start
- 2012-08-27
- Marketing end
- 0000-00-00
- Substance
- FENOPROFEN CALCIUM
- Active strength
- 400 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1302-1 | 71335130201 | 30 CAPSULE in 1 BOTTLE (71335-1302-1) | 30 capsule | 2012-08-27 | 0000-00-00 | No | No | Current |
| 71335-1302-2 | 71335130202 | 90 CAPSULE in 1 BOTTLE (71335-1302-2) | 90 capsule | 2012-08-27 | 0000-00-00 | No | No | Current |