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Grama Grass - 36987-2322-2 - (Grama Grass)

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Drug Information of Grama Grass

Product NDC: 36987-2322
Proprietary Name: Grama Grass
Non Proprietary Name: Grama Grass
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   Grama Grass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Grama Grass

Product NDC: 36987-2322
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Grama Grass

Package NDC: 36987-2322-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-2322-2)

NDC Information of Grama Grass

NDC Code 36987-2322-2
Proprietary Name Grama Grass
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-2322-2)
Product NDC 36987-2322
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Grama 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 BOUTELOUA GRACILIS POLLEN
Strength Number 10000
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 Grama Grass


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