"22840-1363-1" National Drug Code (NDC)

Rough Redroot Rough Redroot 5 mL in 1 VIAL, MULTI-DOSE (22840-1363-1)
(Greer Laboratories, Inc.)

NDC Code22840-1363-1
Package Description5 mL in 1 VIAL, MULTI-DOSE (22840-1363-1)
Product NDC22840-1363
Product Type NameNON-STANDARDIZED ALLERGENIC
Proprietary NameRough Redroot Rough Redroot
Non-Proprietary NameAmaranthus Retroflexus
Dosage FormSOLUTION
UsageINTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date19810915
Marketing Category NameBLA
Application NumberBLA101833
ManufacturerGreer Laboratories, Inc.
Substance NameAMARANTHUS RETROFLEXUS POLLEN
Strength.001
Strength Unitg/mL
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]

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