FLURESS

Product NDC

17478-640

11-digit product format

174780640

Labeler code

17478

Product ID

17478-640_c2b61c86-a6d8-4c09-83f9-6bb7dc12d382

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluorescein Sodium and Benoxinate Hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Akorn, Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

1995-02-01

Marketing end

0000-00-00

Substance

FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE

Active strength

3 mg/mL; mg/mL

Pharmacologic classes

Diagnostic Dye [EPC],Dyes [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record