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"50436-0999-1" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (50436-0999-1)
(Unit Dose Services)

NDC Code50436-0999-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50436-0999-1)
Product NDC50436-0999
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerUnit Dose Services
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/50436-0999-1





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