"49288-0290-3" National Drug Code (NDC)

Lentil 10 mL in 1 VIAL, MULTI-DOSE (49288-0290-3)
(Antigen Laboratories, Inc.)

NDC Code49288-0290-3
Package Description10 mL in 1 VIAL, MULTI-DOSE (49288-0290-3)
Product NDC49288-0290
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLentil
Non-Proprietary NameLentil
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740323
Marketing Category NameBLA
Application NumberBLA102223
ManufacturerAntigen Laboratories, Inc.
Substance NameLENTIL
Strength.05
Strength Unitg/mL
Pharmacy ClassesNon-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Dietary Proteins [CS],Plant Proteins [CS],Allergens [CS]

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