Lipiodol Ultra-Fluide

Product NDC

60694-1901

11-digit product format

606941901

Labeler code

60694

Product ID

60694-1901_7d77b913-ed6f-d441-e053-2991aa0a20ce

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ethiodized Oil

Dosage form

INJECTION

Route

INTRA-ARTERIAL; INTRALYMPHATIC; INTRAMUSCULAR

Labeler

Delpharm Tours

Marketing category

UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE

Marketing start

2015-06-01

Marketing end

0000-00-00

Substance

ETHIODIZED OIL

Active strength

480 mg/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record