Cladribine (Fresenius Kabi USA, LLC)


Welcome to the PulseAid listing for the Cladribine drug offered from Fresenius Kabi USA, LLC. This Purine Antimetabolite [EPC] 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: CLADRIBINE
SUBSTANCE NAME: CLADRIBINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Purine Antimetabolite [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2004-12-01
END MARKETING DATE: 0000-00-00


Cladribine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCladribine from Fresenius Kabi USA, LLC
LABELER NAME: Fresenius Kabi USA, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/mL)
START MARKETING DATE: 2004-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63323-140_bf171945-d77a-4e9a-a4f1-de363d946c0f
PRODUCT NDC: 63323-140
APPLICATION NUMBER: ANDA076571

Other CLADRIBINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Fresenius Kabi USA, LLCCladribine
Mylan Institutional LLCCladribine
Pfizer Laboratories Div Pfizer Inc.Cladribine