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"72162-1737-0" National Drug Code (NDC)

Famotidine 1000 TABLET in 1 BOTTLE (72162-1737-0)
(Bryant Ranch Prepack)

NDC Code72162-1737-0
Package Description1000 TABLET in 1 BOTTLE (72162-1737-0)
Product NDC72162-1737
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerBryant Ranch Prepack
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/72162-1737-0





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