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Iodine Bush - 36987-3228-4 - (Iodine Bush)

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Drug Information of Iodine Bush

Product NDC: 36987-3228
Proprietary Name: Iodine Bush
Non Proprietary Name: Iodine Bush
Active Ingredient(s): .1    g/mL & nbsp;   Iodine Bush
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Iodine Bush

Product NDC: 36987-3228
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Iodine Bush

Package NDC: 36987-3228-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3228-4)

NDC Information of Iodine Bush

NDC Code 36987-3228-4
Proprietary Name Iodine Bush
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3228-4)
Product NDC 36987-3228
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Iodine Bush
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ALLENROLFEA OCCIDENTALIS POLLEN
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Iodine Bush


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