ISOVUE

Product NDC

76381-317

11-digit product format

763810317

Labeler code

76381

Product ID

76381-317_31076157-8a24-15d8-2f7d-343ddf017bff

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

IOPAMIDOL

Dosage form

INJECTION, SOLUTION

Route

INTRAVASCULAR

Labeler

BIPSO GmbH

Application

NDA020327

Marketing category

NDA

Marketing start

1994-10-12

Marketing end

0000-00-00

Substance

IOPAMIDOL

Active strength

510 mg/mL

Pharmacologic classes

Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record