Tobramycin - 50436-1008-1 - (Tobramycin)

Alphabetical Index


Drug Information of Tobramycin

Product NDC: 50436-1008
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: 50436-1008
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062535
Marketing Category: ANDA
Start Marketing Date: 19950109

Package Information of Tobramycin

Package NDC: 50436-1008-1
Package Description: 5 mL in 1 BOTTLE (50436-1008-1)

NDC Information of Tobramycin

NDC Code 50436-1008-1
Proprietary Name Tobramycin
Package Description 5 mL in 1 BOTTLE (50436-1008-1)
Product NDC 50436-1008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tobramycin
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19950109
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name TOBRAMYCIN
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Tobramycin


General Information