PROCRIT - 59676-310-02 - (Erythropoietin)

Alphabetical Index


Drug Information of PROCRIT

Product NDC: 59676-310
Proprietary Name: PROCRIT
Non Proprietary Name: Erythropoietin
Active Ingredient(s): 10000    [iU]/mL & nbsp;   Erythropoietin
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PROCRIT

Product NDC: 59676-310
Labeler Name: Janssen Products, LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103234
Marketing Category: BLA
Start Marketing Date: 19890601

Package Information of PROCRIT

Package NDC: 59676-310-02
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) > 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00)

NDC Information of PROCRIT

NDC Code 59676-310-02
Proprietary Name PROCRIT
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) > 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00)
Product NDC 59676-310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythropoietin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19890601
Marketing Category Name BLA
Labeler Name Janssen Products, LP
Substance Name ERYTHROPOIETIN
Strength Number 10000
Strength Unit [iU]/mL
Pharmaceutical Classes Erythropoiesis-stimulating Agent [EPC],Erythropoietin [Chemical/Ingredient],Increased Erythroid Cell Production [PE]

Complete Information of PROCRIT


General Information