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"69853-0102-1" National Drug Code (NDC)
Andexxa 4 VIAL, SINGLE-USE in 1 CARTON (69853-0102-1) / 20 mL in 1 VIAL, SINGLE-USE
(Alexion Pharmaceuticals, Inc.)
NDC Code
69853-0102-1
Package Description
4 VIAL, SINGLE-USE in 1 CARTON (69853-0102-1) / 20 mL in 1 VIAL, SINGLE-USE
Product NDC
69853-0102
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Andexxa
Non-Proprietary Name
Andexanet Alfa
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20190108
End Marketing Date
20241130
Marketing Category Name
BLA
Application Number
BLA125586
Manufacturer
Alexion Pharmaceuticals, Inc.
Substance Name
ANDEXANET ALFA
Strength
200
Strength Unit
mg/20mL
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69853-0102-1