Infergen - 66435-202-09 - (Interferon alfacon-1)

Alphabetical Index


Drug Information of Infergen

Product NDC: 66435-202
Proprietary Name: Infergen
Non Proprietary Name: Interferon alfacon-1
Active Ingredient(s): .03    mg/mL & nbsp;   Interferon alfacon-1
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Infergen

Product NDC: 66435-202
Labeler Name: Kadmon Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103663
Marketing Category: BLA
Start Marketing Date: 19971006

Package Information of Infergen

Package NDC: 66435-202-09
Package Description: 6 VIAL, SINGLE-DOSE in 1 PACKAGE (66435-202-09) > .3 mL in 1 VIAL, SINGLE-DOSE (66435-202-95)

NDC Information of Infergen

NDC Code 66435-202-09
Proprietary Name Infergen
Package Description 6 VIAL, SINGLE-DOSE in 1 PACKAGE (66435-202-09) > .3 mL in 1 VIAL, SINGLE-DOSE (66435-202-95)
Product NDC 66435-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Interferon alfacon-1
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 19971006
Marketing Category Name BLA
Labeler Name Kadmon Pharmaceuticals, LLC
Substance Name INTERFERON ALFACON-1
Strength Number .03
Strength Unit mg/mL
Pharmaceutical Classes Interferon alpha [EPC],Interferon-alpha [Chemical/Ingredient]

Complete Information of Infergen


General Information