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Annual Blue Grass - 36987-2278-4 - (Annual Blue Grass)

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Drug Information of Annual Blue Grass

Product NDC: 36987-2278
Proprietary Name: Annual Blue Grass
Non Proprietary Name: Annual Blue Grass
Active Ingredient(s): .1    g/mL & nbsp;   Annual Blue Grass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Annual Blue Grass

Product NDC: 36987-2278
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Annual Blue Grass

Package NDC: 36987-2278-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2278-4)

NDC Information of Annual Blue Grass

NDC Code 36987-2278-4
Proprietary Name Annual Blue Grass
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2278-4)
Product NDC 36987-2278
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Annual Blue 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 POA ANNUA POLLEN
Strength Number .1
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 Annual Blue Grass


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