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HONEY BEE VENOM - 52709-0801-2 - (APIS MELLIFERA VENOM)

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Drug Information of HONEY BEE VENOM

Product NDC: 52709-0801
Proprietary Name: HONEY BEE VENOM
Non Proprietary Name: APIS MELLIFERA VENOM
Active Ingredient(s): 120    ug/1 & nbsp;   APIS MELLIFERA VENOM
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HONEY BEE VENOM

Product NDC: 52709-0801
Labeler Name: ALK-Abello A S
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103969
Marketing Category: BLA
Start Marketing Date: 19921120

Package Information of HONEY BEE VENOM

Package NDC: 52709-0801-2
Package Description: 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (52709-0801-2)

NDC Information of HONEY BEE VENOM

NDC Code 52709-0801-2
Proprietary Name HONEY BEE VENOM
Package Description 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (52709-0801-2)
Product NDC 52709-0801
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name APIS MELLIFERA VENOM
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19921120
Marketing Category Name BLA
Labeler Name ALK-Abello A S
Substance Name APIS MELLIFERA VENOM
Strength Number 120
Strength Unit ug/1
Pharmaceutical Classes

Complete Information of HONEY BEE VENOM


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