Cladribine (Pfizer Laboratories Div Pfizer Inc.)


Welcome to the PulseAid listing for the Cladribine drug offered from Pfizer Laboratories Div Pfizer Inc.. 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: Pfizer Laboratories Div Pfizer Inc.
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: 2011-07-10
END MARKETING DATE: 0000-00-00


Cladribine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCladribine from Pfizer Laboratories Div Pfizer Inc.
LABELER NAME: Pfizer Laboratories Div Pfizer Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/mL)
START MARKETING DATE: 2011-07-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0069-0086_5a1b9efb-8d26-43a1-909b-d59ca0dc382a
PRODUCT NDC: 0069-0086
APPLICATION NUMBER: ANDA200510

Other CLADRIBINE Pharmaceutical Manufacturers / Labelers:

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