Tobramycin - 63323-306-02 - (TOBRAMYCIN SULFATE)

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Drug Information of Tobramycin

Product NDC: 63323-306
Proprietary Name: Tobramycin
Non Proprietary Name: TOBRAMYCIN SULFATE
Active Ingredient(s): 40    mg/mL & nbsp;   TOBRAMYCIN SULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tobramycin

Product NDC: 63323-306
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065122
Marketing Category: ANDA
Start Marketing Date: 20051123

Package Information of Tobramycin

Package NDC: 63323-306-02
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (63323-306-02) > 2 mL in 1 VIAL, MULTI-DOSE

NDC Information of Tobramycin

NDC Code 63323-306-02
Proprietary Name Tobramycin
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (63323-306-02) > 2 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-306
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TOBRAMYCIN SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20051123
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name TOBRAMYCIN SULFATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Tobramycin


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