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"50436-7370-1" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (50436-7370-1)
(Unit Dose Services)

NDC Code50436-7370-1
Package Description30 TABLET in 1 BOTTLE (50436-7370-1)
Product NDC50436-7370
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerUnit Dose Services
Substance NameFAMOTIDINE
Strength40
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/50436-7370-1





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