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Rabbit Bush - 49288-0208-4 - (Rabbit Bush)

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Drug Information of Rabbit Bush

Product NDC: 49288-0208
Proprietary Name: Rabbit Bush
Non Proprietary Name: Rabbit Bush
Active Ingredient(s): .05    g/mL & nbsp;   Rabbit Bush
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rabbit Bush

Product NDC: 49288-0208
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Rabbit Bush

Package NDC: 49288-0208-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0208-4)

NDC Information of Rabbit Bush

NDC Code 49288-0208-4
Proprietary Name Rabbit Bush
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0208-4)
Product NDC 49288-0208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rabbit Bush
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name AMBROSIA DELTOIDEA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Rabbit Bush


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