Folotyn - 48818-001-02 - (pralatrexate)

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Drug Information of Folotyn

Product NDC: 48818-001
Proprietary Name: Folotyn
Non Proprietary Name: pralatrexate
Active Ingredient(s): 20    mg/mL & nbsp;   pralatrexate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Folotyn

Product NDC: 48818-001
Labeler Name: Allos Therapeutics
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022468
Marketing Category: NDA
Start Marketing Date: 20090924

Package Information of Folotyn

Package NDC: 48818-001-02
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (48818-001-02) > 2 mL in 1 VIAL, SINGLE-USE

NDC Information of Folotyn

NDC Code 48818-001-02
Proprietary Name Folotyn
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (48818-001-02) > 2 mL in 1 VIAL, SINGLE-USE
Product NDC 48818-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pralatrexate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20090924
Marketing Category Name NDA
Labeler Name Allos Therapeutics
Substance Name PRALATREXATE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC]

Complete Information of Folotyn


General Information