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American Elm - 36987-2631-4 - (American Elm)

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Drug Information of American Elm

Product NDC: 36987-2631
Proprietary Name: American Elm
Non Proprietary Name: American Elm
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   American Elm
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of American Elm

Product NDC: 36987-2631
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of American Elm

Package NDC: 36987-2631-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2631-4)

NDC Information of American Elm

NDC Code 36987-2631-4
Proprietary Name American Elm
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2631-4)
Product NDC 36987-2631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name American Elm
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ULMUS AMERICANA POLLEN
Strength Number 20000
Strength Unit [PNU]/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 American Elm


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