MOXEZA

Product NDC
0065-0006
11-digit product format
000650006
Labeler code
0065
Product ID
0065-0006_ba96c083-00b4-4b6f-8aa0-327e9e918461
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
moxifloxacin hydrochloride
Dosage form
SOLUTION
Route
OPHTHALMIC
Labeler
Alcon Laboratories, Inc.
Application
NDA022428
Marketing category
NDA
Marketing start
2011-01-18
Marketing end
0000-00-00
Substance
MOXIFLOXACIN HYDROCHLORIDE
Active strength
5 mg/mL
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0065-0006-032025-12-31C16284748780-1f386c649-d91c-0266-e053-dadaa90a7c1a05248b68-16a9-488d-a39f-5137d2410471
0065-0006-032023-01-30C16284748780-1f386c649-d91c-0266-e053-dadaa90a7c1a05248b68-16a9-488d-a39f-5137d2410471

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0065-0006-03ML - Milliliter0065-0006934628f8-41b4-4a77-9c3d-9a926ccdae1412012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0065-0006MOXEZA (MOXIFLOXACIN HYDROCHLORIDE) SOLUTION [ALCON LABORATORIES, INC.]20Legacy NDC20210820_05248b68-16a9-488d-a39f-5137d2410471.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0065-0006-03000650006033 mL in 1 BOTTLE (0065-0006-03) 3 ml2011-01-180000-00-00NoNoCurrent