"22840-2337-2" National Drug Code (NDC)

Rough Redroot Rough Redroot 10 mL in 1 VIAL, MULTI-DOSE (22840-2337-2)
(Greer Laboratories, Inc.)

NDC Code22840-2337-2
Package Description10 mL in 1 VIAL, MULTI-DOSE (22840-2337-2)
Product NDC22840-2337
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.1
Strength Unitg/mL
Pharmacy ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS]

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