"49643-309-50" National Drug Code (NDC)

Standardized Redtop Grass 50 mL in 1 VIAL, MULTI-DOSE (49643-309-50)
(Allermed Laboratories, Inc.)

NDC Code49643-309-50
Package Description50 mL in 1 VIAL, MULTI-DOSE (49643-309-50)
Product NDC49643-309
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameStandardized Redtop Grass
Non-Proprietary NameAgrostis Alba
Dosage FormINJECTION
UsageCUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date19961202
Marketing Category NameBLA
Application NumberBLA102218
ManufacturerAllermed Laboratories, Inc.
Substance NameAGROSTIS GIGANTEA POLLEN
Strength100000
Strength Unit[BAU]/mL
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS], Standardized Pollen Allergenic Extract [EPC]

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