Nalfon
- Product NDC
- 42195-308
- 11-digit product format
- 421950308
- Labeler code
- 42195
- Product ID
- 42195-308_f03034a3-a06c-4446-e053-2995a90a58fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenoprofen calcium
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Xspire Pharma
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42195-308-09 | 42195030809 | 90 CAPSULE in 1 BOTTLE (42195-308-09) | 90 capsule | 2012-08-27 | 0000-00-00 | No | No | Current |
| 42195-308-60 | 42195030860 | 60 CAPSULE in 1 BOTTLE (42195-308-60) | 60 capsule | 2019-03-25 | 0000-00-00 | No | No | Current |