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Quack Grass - 36987-2361-2 - (Quack Grass)

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Drug Information of Quack Grass

Product NDC: 36987-2361
Proprietary Name: Quack Grass
Non Proprietary Name: Quack Grass
Active Ingredient(s): .05    g/mL & nbsp;   Quack Grass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Quack Grass

Product NDC: 36987-2361
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Quack Grass

Package NDC: 36987-2361-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-2361-2)

NDC Information of Quack Grass

NDC Code 36987-2361-2
Proprietary Name Quack Grass
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-2361-2)
Product NDC 36987-2361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quack Grass
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ELYMUS REPENS 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 Quack Grass


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