TOBREX - 0065-0644-35 - (tobramycin)

Alphabetical Index


Drug Information of TOBREX

Product NDC: 0065-0644
Proprietary Name: TOBREX
Non Proprietary Name: tobramycin
Active Ingredient(s): 3    mg/g & nbsp;   tobramycin
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of TOBREX

Product NDC: 0065-0644
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050555
Marketing Category: NDA
Start Marketing Date: 19810628

Package Information of TOBREX

Package NDC: 0065-0644-35
Package Description: 3.5 g in 1 TUBE (0065-0644-35)

NDC Information of TOBREX

NDC Code 0065-0644-35
Proprietary Name TOBREX
Package Description 3.5 g in 1 TUBE (0065-0644-35)
Product NDC 0065-0644
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tobramycin
Dosage Form Name OINTMENT
Route Name OPHTHALMIC
Start Marketing Date 19810628
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc.
Substance Name TOBRAMYCIN
Strength Number 3
Strength Unit mg/g
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of TOBREX


General Information