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"58593-781-02" National Drug Code (NDC)
Finafta 7100 mg in 1 TUBE (58593-781-02)
(Efficient Laboratories Inc.)
NDC Code
58593-781-02
Package Description
7100 mg in 1 TUBE (58593-781-02)
Product NDC
58593-781
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Finafta
Proprietary Name Suffix
Baby
Non-Proprietary Name
Benzocaine
Dosage Form
LIQUID
Usage
ORAL
Start Marketing Date
20000101
Marketing Category Name
OTC MONOGRAPH NOT FINAL
Application Number
part356
Manufacturer
Efficient Laboratories Inc.
Substance Name
BENZOCAINE
Strength
7.5
Strength Unit
mg/100mg
Pharmacy Classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58593-781-02