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Black Birch - 36987-2547-4 - (Black Birch)

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Drug Information of Black Birch

Product NDC: 36987-2547
Proprietary Name: Black Birch
Non Proprietary Name: Black Birch
Active Ingredient(s): .05    g/mL & nbsp;   Black Birch
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Black Birch

Product NDC: 36987-2547
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Black Birch

Package NDC: 36987-2547-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2547-4)

NDC Information of Black Birch

NDC Code 36987-2547-4
Proprietary Name Black Birch
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2547-4)
Product NDC 36987-2547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Black Birch
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BETULA LENTA POLLEN
Strength Number .05
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 Black Birch


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