Gati-Dex

Product NDC
71384-506
11-digit product format
713840506
Labeler code
71384
Product ID
71384-506_638a1f49-53e8-7a69-e053-2991aa0a82bc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gatifloxacin-Dexamethasone Phosphate
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Imprimis NJOF, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-01-05
Marketing end
0000-00-00
Substance
DEXAMETHASONE SODIUM PHOSPHATE; GATIFLOXACIN
Active strength
1 mg/mL; mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Quinolone Antimicrobial [EPC],Quinolones [CS]
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
71384-506-052020-02-12C16284748780-19d75b9d0-9541-f424-e053-dadaa90a57ce6325d560-cd47-fc9b-e053-2991aa0a719e
71384-506-052020-01-31C16284748780-19d75b9d0-9541-f424-e053-dadaa90a57ce6325d560-cd47-fc9b-e053-2991aa0a719e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71384-506-05ML - Milliliter71384-506c4d872a8-45e5-4ad9-8427-c0c9f335a1da12018-07-03