Tobramycin - 52959-108-03 - (Tobramycin)

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Drug Information of Tobramycin

Product NDC: 52959-108
Proprietary Name: Tobramycin
Non Proprietary Name: Tobramycin
Active Ingredient(s): 3    mg/mL & nbsp;   Tobramycin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tobramycin

Product NDC: 52959-108
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064052
Marketing Category: ANDA
Start Marketing Date: 19931129

Package Information of Tobramycin

Package NDC: 52959-108-03
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (52959-108-03) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Tobramycin

NDC Code 52959-108-03
Proprietary Name Tobramycin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (52959-108-03) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 52959-108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tobramycin
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19931129
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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