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"36987-2659-4" National Drug Code (NDC)

Eucalyptus 50 mL in 1 VIAL, MULTI-DOSE (36987-2659-4)
(Nelco Laboratories, Inc.)

NDC Code36987-2659-4
Package Description50 mL in 1 VIAL, MULTI-DOSE (36987-2659-4)
Product NDC36987-2659
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEucalyptus
Non-Proprietary NameEucalyptus
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19720829
Marketing Category NameBLA
Application NumberBLA102192
ManufacturerNelco Laboratories, Inc.
Substance NameEUCALYPTUS GLOBULUS POLLEN
Strength.05
Strength Unitg/mL
Pharmacy ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]

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