Vexol

Product NDC
0065-0627
11-digit product format
000650627
Labeler code
0065
Product ID
0065-0627_047301fe-73f6-356c-ec16-a1123037f239
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
rimexolone
Dosage form
SUSPENSION/ DROPS
Route
OPHTHALMIC
Labeler
Alcon Laboratories, Inc
Application
NDA020474
Marketing category
NDA
Marketing start
1995-09-15
Marketing end
0000-00-00
Substance
RIMEXOLONE
Active strength
10 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0065-0627-03ML - Milliliter0065-062773b4f1fb-a176-40b9-9ac6-ced3b2108b2512012-07-24
0065-0627-07ML - Milliliter0065-0627117e7cb0-f70d-4c5e-b89c-e24de2b953cc12012-07-24