"36987-1319-4" National Drug Code (NDC)

Date 50 mL in 1 VIAL, MULTI-DOSE (36987-1319-4)
(Nelco Laboratories, Inc.)

NDC Code36987-1319-4
Package Description50 mL in 1 VIAL, MULTI-DOSE (36987-1319-4)
Product NDC36987-1319
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDate
Non-Proprietary NameDate
Dosage FormINJECTION, SOLUTION
UsageINTRADERMAL; SUBCUTANEOUS
Start Marketing Date19720829
Marketing Category NameBLA
Application NumberBLA102192
ManufacturerNelco Laboratories, Inc.
Substance NameDATE
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],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Fruit Proteins [EXT]

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