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"59368-288-01" National Drug Code (NDC)

Sunmark Acid Reducer 1 BOTTLE in 1 CARTON (59368-288-01) / 50 TABLET, FILM COATED in 1 BOTTLE
(Praxis, LLC)

NDC Code59368-288-01
Package Description1 BOTTLE in 1 CARTON (59368-288-01) / 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC59368-288
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Acid Reducer
Proprietary Name SuffixMaximum Strength
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070618
End Marketing Date20250401
Marketing Category NameANDA
Application NumberANDA077351
ManufacturerPraxis, LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59368-288-01





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