ALTAFLUOR

Product NDC
59390-206
11-digit product format
593900206
Labeler code
59390
Product ID
59390-206_3f415ffe-f95c-418b-9ee3-a1e34670a4e5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluorescein Sodium and Benoxinate Hydrochloride
Dosage form
SOLUTION
Route
OPHTHALMIC
Labeler
Altaire Pharmaceuticals Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2000-06-21
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59390-206-05ML - Milliliter59390-206402da5f1-6ccd-433d-9f37-f56f36ca149112014-06-03