"59368-236-01" National Drug Code (NDC)

Berkley And Jensen Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (59368-236-01)
(Praxis, LLC)

NDC Code59368-236-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (59368-236-01)
Product NDC59368-236
Product Type NameHUMAN OTC DRUG
Proprietary NameBerkley And Jensen Famotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131209
Marketing Category NameANDA
Application NumberANDA077351
ManufacturerPraxis, LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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