KANAMYCIN (Fresenius Kabi USA, LLC)


Welcome to the PulseAid listing for the KANAMYCIN drug offered from Fresenius Kabi USA, LLC. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Fresenius Kabi USA, LLC
NON-PROPRIETARY NAME: KANAMYCIN
SUBSTANCE NAME: KANAMYCIN A SULFATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAMUSCULAR; INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2003-01-28
END MARKETING DATE: 0000-00-00


KANAMYCIN HUMAN PRESCRIPTION DRUG Details:

Item DescriptionKANAMYCIN from Fresenius Kabi USA, LLC
LABELER NAME: Fresenius Kabi USA, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 333(mg/mL)
START MARKETING DATE: 2003-01-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63323-359_d50696cd-0f4c-4ba0-a0bf-3af5159ab17e
PRODUCT NDC: 63323-359
APPLICATION NUMBER: ANDA065111

Other KANAMYCIN A SULFATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Fresenius Kabi USA, LLCKANAMYCIN