"36987-2217-1" National Drug Code (NDC)

Flaxseed 5 mL in 1 VIAL, MULTI-DOSE (36987-2217-1)
(Nelco Laboratories, Inc.)

NDC Code36987-2217-1
Package Description5 mL in 1 VIAL, MULTI-DOSE (36987-2217-1)
Product NDC36987-2217
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFlaxseed
Non-Proprietary NameFlaxseed
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19720829
Marketing Category NameBLA
Application NumberBLA102192
ManufacturerNelco Laboratories, Inc.
Substance NameFLAX SEED
Strength20000
Strength Unit[PNU]/mL
Pharmacy ClassesNon-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS]

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