BioThrax - 64678-211-01 - (BACILLUS ANTHRACIS)

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Drug Information of BioThrax

Product NDC: 64678-211
Proprietary Name: BioThrax
Non Proprietary Name: BACILLUS ANTHRACIS
Active Ingredient(s): 100    ug/mL & nbsp;   BACILLUS ANTHRACIS
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of BioThrax

Product NDC: 64678-211
Labeler Name: Emergent BioDefense Operations Lansing, LLC
Product Type: VACCINE
FDA Application Number: BLA103821
Marketing Category: BLA
Start Marketing Date: 19701104

Package Information of BioThrax

Package NDC: 64678-211-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (64678-211-01) > 5 mL in 1 VIAL, MULTI-DOSE (64678-211-05)

NDC Information of BioThrax

NDC Code 64678-211-01
Proprietary Name BioThrax
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (64678-211-01) > 5 mL in 1 VIAL, MULTI-DOSE (64678-211-05)
Product NDC 64678-211
Product Type Name VACCINE
Non Proprietary Name BACILLUS ANTHRACIS
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 19701104
Marketing Category Name BLA
Labeler Name Emergent BioDefense Operations Lansing, LLC
Substance Name BACILLUS ANTHRACIS STRAIN V770-NP1-R ANTIGENS
Strength Number 100
Strength Unit ug/mL
Pharmaceutical Classes Live Attenuated Bacillus Anthracis Vaccine [EPC],Actively Acquired Immunity [PE],Vaccines, Attenuated [Chemical/Ingredient],Anthrax Vaccines [Chemical/Ingredient]

Complete Information of BioThrax


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