NDC 0187-0650

Oxsoralen-Ultra

Methoxsalen

Oxsoralen-Ultra is a Oral Capsule, Liquid Filled in the Human Prescription Drug category. It is labeled and distributed by Bausch Health Us, Llc. The primary component is Methoxsalen.

• Product ID: 0187-0650_0fed5b76-59f5-4e9a-ba0c-6569e9561daf
• NDC: 0187-0650
• Product Type: Human Prescription Drug
• Proprietary Name: Oxsoralen-Ultra
• Generic Name: Methoxsalen
• Dosage Form: Capsule, Liquid Filled
• Route of Administration: ORAL
• Marketing Start Date: 1986-10-30
• Marketing Category: NDA / NDA
• Application Number: NDA019600
• Labeler Name: Bausch Health US, LLC
• Substance Name: METHOXSALEN
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: Psoralen [EPC],Psoralens [CS],Photoabsorption [MoA],Photoactivated Radical Generator [EPC],Photosensitizing Activity [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0187-0650-42

50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0187-0650-42)

• Marketing Start Date: 1986-10-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0187-0650-42 [00187065042]

Oxsoralen-Ultra CAPSULE, LIQUID FILLED

• Marketing Category: NDA
• Application Number: NDA019600
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1986-10-30

Drug Details

Active Ingredients

Ingredient	Strength
METHOXSALEN	10 mg/1

OpenFDA Data

• SPL SET ID: ae951dc4-9031-43bf-943c-cb2366951f23
• Manufacturer:
  • Valeant Pharmaceuticals North America LLC
• UNII:
  • U4VJ29L7BQ
• RxNorm Concept Unique ID - RxCUI:
  • 1812434
  • 207074

Pharmacological Class

• Psoralen [EPC]
• Psoralens [CS]
• Photoabsorption [MoA]
• Photoactivated Radical Generator [EPC]
• Photosensitizing Activity [PE]

NDC Crossover Matching brand name "Oxsoralen-Ultra" or generic name "Methoxsalen"

NDC	Brand Name	Generic Name
0187-0650	Oxsoralen-Ultra	Methoxsalen
45963-325	Methoxsalen	Methoxsalen
64380-752	Methoxsalen	Methoxsalen
68682-065	Methoxsalen	Methoxsalen
64067-216	UVADEX	Methoxsalen