Nalfon
- Product NDC
- 42195-600
- 11-digit product format
- 421950600
- Labeler code
- 42195
- Product ID
- 42195-600_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
- 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
- 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 |
|---|
| 42195-600-10 | 42195060010 | 100 CAPSULE in 1 BOTTLE (42195-600-10) | 100 capsule | 2012-08-27 | 0000-00-00 | No | No | Current |