TobraDex - 21695-628-35 - (tobramycin and dexamethasone)

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Drug Information of TobraDex

Product NDC: 21695-628
Proprietary Name: TobraDex
Non Proprietary Name: tobramycin and dexamethasone
Active Ingredient(s): 1; 3    mg/g; mg/g & nbsp;   tobramycin and dexamethasone
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of TobraDex

Product NDC: 21695-628
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050616
Marketing Category: NDA
Start Marketing Date: 19880928

Package Information of TobraDex

Package NDC: 21695-628-35
Package Description: 3.5 g in 1 TUBE (21695-628-35)

NDC Information of TobraDex

NDC Code 21695-628-35
Proprietary Name TobraDex
Package Description 3.5 g in 1 TUBE (21695-628-35)
Product NDC 21695-628
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tobramycin and dexamethasone
Dosage Form Name OINTMENT
Route Name OPHTHALMIC
Start Marketing Date 19880928
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name DEXAMETHASONE; TOBRAMYCIN
Strength Number 1; 3
Strength Unit mg/g; mg/g
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of TobraDex


General Information