Tobramycin - 17478-290-10 - (Tobramycin)

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Drug Information of Tobramycin

Product NDC: 17478-290
Proprietary Name: Tobramycin
Non Proprietary Name: Tobramycin
Active Ingredient(s): 3    mg/mL & nbsp;   Tobramycin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Tobramycin

Product NDC: 17478-290
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064096
Marketing Category: ANDA
Start Marketing Date: 19960131

Package Information of Tobramycin

Package NDC: 17478-290-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-290-10) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Tobramycin

NDC Code 17478-290-10
Proprietary Name Tobramycin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-290-10) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 17478-290
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tobramycin
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19960131
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name TOBRAMYCIN
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Tobramycin


General Information