Tobramycin - 52125-232-01 - (Tobramycin)

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Drug Information of Tobramycin

Product NDC: 52125-232
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: 52125-232
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064096
Marketing Category: ANDA
Start Marketing Date: 20130613

Package Information of Tobramycin

Package NDC: 52125-232-01
Package Description: 5 mL in 1 BOTTLE, DROPPER (52125-232-01)

NDC Information of Tobramycin

NDC Code 52125-232-01
Proprietary Name Tobramycin
Package Description 5 mL in 1 BOTTLE, DROPPER (52125-232-01)
Product NDC 52125-232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tobramycin
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130613
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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