NDC 60694-1901

Lipiodol Ultra-Fluide

Ethiodized Oil

Lipiodol Ultra-Fluide is a Intra-arterial; Intralymphatic; Intramuscular Injection in the Human Prescription Drug category. It is labeled and distributed by Delpharm Tours. The primary component is Ethiodized Oil.

• Product ID: 60694-1901_7d77b913-ed6f-d441-e053-2991aa0a20ce
• NDC: 60694-1901
• Product Type: Human Prescription Drug
• Proprietary Name: Lipiodol Ultra-Fluide
• Generic Name: Ethiodized Oil
• Dosage Form: Injection
• Route of Administration: INTRA-ARTERIAL; INTRALYMPHATIC; INTRAMUSCULAR
• Marketing Start Date: 2015-06-01
• Marketing Category: UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE / UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
• Labeler Name: Delpharm Tours
• Substance Name: ETHIODIZED OIL
• Active Ingredient Strength: 480 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60694-1901-0

1 AMPULE in 1 CARTON (60694-1901-0) > 10 mL in 1 AMPULE

• Marketing Start Date: 2015-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60694-1901-0 [60694190100]

Lipiodol Ultra-Fluide INJECTION

• Marketing Category: Unapproved drug for use in drug shor
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-06-01
• Marketing End Date: 2019-04-01

Drug Details

Active Ingredients

Ingredient	Strength
ETHIODIZED OIL	480 mg/mL

OpenFDA Data

• SPL SET ID: f3d37e9c-2f30-4716-9217-bdf5253b0800
• Manufacturer:
  • Delpharm Tours
• UNII:
  • KZW0R0686Q

NDC Crossover Matching brand name "Lipiodol Ultra-Fluide" or generic name "Ethiodized Oil"

NDC	Brand Name	Generic Name
60694-1901	Lipiodol Ultra-Fluide	Ethiodized Oil
67684-1901	LIPIODOL	ethiodized oil