"49288-0052-5" National Drug Code (NDC)

Beet 50 mL in 1 VIAL, MULTI-DOSE (49288-0052-5)
(Antigen Laboratories, Inc.)

NDC Code49288-0052-5
Package Description50 mL in 1 VIAL, MULTI-DOSE (49288-0052-5)
Product NDC49288-0052
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBeet
Non-Proprietary NameBeet
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740323
Marketing Category NameBLA
Application NumberBLA102223
ManufacturerAntigen Laboratories, Inc.
Substance NameBEET
Strength.05
Strength Unitg/mL
Pharmacy ClassesNon-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Vegetable Proteins [CS]

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