"49288-0460-3" National Drug Code (NDC)

Sorrel Mixture 10 mL in 1 VIAL, MULTI-DOSE (49288-0460-3)
(Antigen Laboratories, Inc.)

NDC Code49288-0460-3
Package Description10 mL in 1 VIAL, MULTI-DOSE (49288-0460-3)
Product NDC49288-0460
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSorrel Mixture
Non-Proprietary NameSorrel Mixture
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740323
Marketing Category NameBLA
Application NumberBLA102223
ManufacturerAntigen Laboratories, Inc.
Substance NameRUMEX OBTUSIFOLIUS POLLEN; RUMEX ACETOSELLA POLLEN; RUMEX ALTISSIMUS POLLEN; RUMEX SALICIFOLIUS VAR. MEXICANUS POLLEN; RUMEX CRISPUS POLLEN
Strength.004; .004; .004; .004; .004
Strength Unitg/mL; g/mL; g/mL; g/mL; g/mL
Pharmacy ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-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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