Methoxsalen
- Product NDC
- 68682-065
- 11-digit product format
- 686820065
- Labeler code
- 68682
- Product ID
- 68682-065_04ad44bf-bf59-4f88-ba31-2a5620883d05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methoxsalen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA019600
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-07-15
- Marketing end
- 0000-00-00
- Substance
- METHOXSALEN
- Active strength
- 10 mg/1
- Pharmacologic classes
- Psoralen [EPC],Psoralens [CS],Photoabsorption [MoA],Photoactivated Radical Generator [EPC],Photosensitizing Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-065-10 | 68682006510 | 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (68682-065-10) | 2014-07-15 | 0000-00-00 | No | No | Current |