"58593-781-02" National Drug Code (NDC)

Finafta 7100 mg in 1 TUBE (58593-781-02)
(Efficient Laboratories Inc.)

NDC Code58593-781-02
Package Description7100 mg in 1 TUBE (58593-781-02)
Product NDC58593-781
Product Type NameHUMAN OTC DRUG
Proprietary NameFinafta
Proprietary Name SuffixBaby
Non-Proprietary NameBenzocaine
Dosage FormLIQUID
UsageORAL
Start Marketing Date20000101
Marketing Category NameOTC MONOGRAPH NOT FINAL
Application Numberpart356
ManufacturerEfficient Laboratories Inc.
Substance NameBENZOCAINE
Strength7.5
Strength Unitmg/100mg
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]

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