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"71335-0231-3" National Drug Code (NDC)

Famotidine 100 TABLET in 1 BOTTLE (71335-0231-3)
(Bryant Ranch Prepack)

NDC Code71335-0231-3
Package Description100 TABLET in 1 BOTTLE (71335-0231-3)
Product NDC71335-0231
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
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/71335-0231-3





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