Kanamycin - 63323-359-03 - (KANAMYCIN A SULFATE)

Alphabetical Index


Drug Information of Kanamycin

Product NDC: 63323-359
Proprietary Name: Kanamycin
Non Proprietary Name: KANAMYCIN A SULFATE
Active Ingredient(s): 333    mg/mL & nbsp;   KANAMYCIN A SULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kanamycin

Product NDC: 63323-359
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065111
Marketing Category: ANDA
Start Marketing Date: 20030128

Package Information of Kanamycin

Package NDC: 63323-359-03
Package Description: 10 VIAL in 1 TRAY (63323-359-03) > 3 mL in 1 VIAL

NDC Information of Kanamycin

NDC Code 63323-359-03
Proprietary Name Kanamycin
Package Description 10 VIAL in 1 TRAY (63323-359-03) > 3 mL in 1 VIAL
Product NDC 63323-359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KANAMYCIN A SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20030128
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name KANAMYCIN A SULFATE
Strength Number 333
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Kanamycin


General Information