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Cultivated Rye - 36987-2369-4 - (Cultivated Rye)

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Drug Information of Cultivated Rye

Product NDC: 36987-2369
Proprietary Name: Cultivated Rye
Non Proprietary Name: Cultivated Rye
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Cultivated Rye
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cultivated Rye

Product NDC: 36987-2369
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Cultivated Rye

Package NDC: 36987-2369-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2369-4)

NDC Information of Cultivated Rye

NDC Code 36987-2369-4
Proprietary Name Cultivated Rye
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2369-4)
Product NDC 36987-2369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cultivated Rye
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name SECALE CEREALE POLLEN
Strength Number 40000
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 Cultivated Rye


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