Fluorescein Sodium and Benoxinate Hydrochloride

Product NDC
24208-732
11-digit product format
242080732
Labeler code
24208
Product ID
24208-732_ca1981e3-3b68-46f9-95b5-db9dc481eaa5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluorescein Sodium and Benoxinate Hydrochloride
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Bausch & Lomb Incorporated
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1995-01-01
Marketing end
0000-00-00
Substance
BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
Active strength
4 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24208-732-05ML - Milliliter24208-732ab01653d-ea20-4040-b041-54aa42fede2612013-02-13