"49288-0436-1" National Drug Code (NDC)

Rhodotorula 2 mL in 1 VIAL, MULTI-DOSE (49288-0436-1)
(Antigen Laboratories, Inc.)

NDC Code49288-0436-1
Package Description2 mL in 1 VIAL, MULTI-DOSE (49288-0436-1)
Product NDC49288-0436
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRhodotorula
Non-Proprietary NameRhodotorula
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740323
Marketing Category NameBLA
Application NumberBLA102223
ManufacturerAntigen Laboratories, Inc.
Substance NameRHODOTORULA RUBRA
Strength.05
Strength Unitg/mL
Pharmacy ClassesNon-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS]

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