"49643-020-30" National Drug Code (NDC)

Orris Root 30 mL in 1 VIAL, MULTI-DOSE (49643-020-30)
(Allermed Laboratories, Inc.)

NDC Code49643-020-30
Package Description30 mL in 1 VIAL, MULTI-DOSE (49643-020-30)
Product NDC49643-020
Product Type NameNON-STANDARDIZED ALLERGENIC
Proprietary NameOrris Root
Non-Proprietary NameOrris Root
Dosage FormINJECTION
UsageCUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date19740312
Marketing Category NameBLA
Application NumberBLA102211
ManufacturerAllermed Laboratories, Inc.
Substance NameIRIS GERMANICA VAR. FLORENTINA ROOT
Strength.1
Strength Unitg/mL
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]

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