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"36987-3020-2" National Drug Code (NDC)

White Poplar 10 mL in 1 VIAL, MULTI-DOSE (36987-3020-2)
(Nelco Laboratories, Inc.)

NDC Code36987-3020-2
Package Description10 mL in 1 VIAL, MULTI-DOSE (36987-3020-2)
Product NDC36987-3020
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameWhite Poplar
Non-Proprietary NameWhite Poplar
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19720829
Marketing Category NameBLA
Application NumberBLA102192
ManufacturerNelco Laboratories, Inc.
Substance NamePOPULUS ALBA POLLEN
Strength.1
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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