Itchy Eye Drops

Product NDC
50804-392
11-digit product format
508040392
Labeler code
50804
Product ID
50804-392_1ea5f150-3375-43ff-965e-5077f8349953
Type
HUMAN OTC DRUG
Nonproprietary name
Ketotifen Fumarate
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Good Sense
Application
ANDA077958
Marketing category
ANDA
Marketing start
2014-06-20
Marketing end
0000-00-00
Substance
KETOTIFEN FUMARATE
Active strength
0 mg/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50804-392-012020-10-21C16284748780-19d75b9d0-a024-f424-e053-dadaa90a57ce61ed30dd-1878-4c8f-bef9-12ad1cc9be86
50804-392-012020-01-31C16284748780-19d75b9d0-a024-f424-e053-dadaa90a57ce61ed30dd-1878-4c8f-bef9-12ad1cc9be86

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50804-392-01ML - Milliliter50804-392b5cab382-8e67-4a99-8363-4aa8a23b3e6012017-08-11