Oxsoralen-Ultra
- Product NDC
- 0187-0650
- 11-digit product format
- 001870650
- Labeler code
- 0187
- Product ID
- 0187-0650_0fed5b76-59f5-4e9a-ba0c-6569e9561daf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methoxsalen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bausch Health US, LLC
- Application
- NDA019600
- Marketing category
- NDA
- Marketing start
- 1986-10-30
- 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
- 2021-12-31
- 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 |
|---|
| 0187-0650-42 | 00187065042 | 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0187-0650-42) | 1986-10-30 | 0000-00-00 | No | No | Current |