Rabbitbush - 36987-3344-4 - (Rabbitbush)

Alphabetical Index


Drug Information of Rabbitbush

Product NDC: 36987-3344
Proprietary Name: Rabbitbush
Non Proprietary Name: Rabbitbush
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Rabbitbush
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rabbitbush

Product NDC: 36987-3344
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Rabbitbush

Package NDC: 36987-3344-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3344-4)

NDC Information of Rabbitbush

NDC Code 36987-3344-4
Proprietary Name Rabbitbush
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3344-4)
Product NDC 36987-3344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rabbitbush
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AMBROSIA DELTOIDEA POLLEN
Strength Number 20000
Strength Unit [PNU]/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 Rabbitbush


General Information