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"49288-0290-3" National Drug Code (NDC)
Lentil 10 mL in 1 VIAL, MULTI-DOSE (49288-0290-3)
(Antigen Laboratories, Inc.)
NDC Code
49288-0290-3
Package Description
10 mL in 1 VIAL, MULTI-DOSE (49288-0290-3)
Product NDC
49288-0290
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lentil
Non-Proprietary Name
Lentil
Dosage Form
INJECTION, SOLUTION
Usage
INTRADERMAL; SUBCUTANEOUS
Start Marketing Date
19740323
Marketing Category Name
BLA
Application Number
BLA102223
Manufacturer
Antigen Laboratories, Inc.
Substance Name
LENTIL
Strength
.05
Strength Unit
g/mL
Pharmacy Classes
Non-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]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49288-0290-3