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"16714-362-05" National Drug Code (NDC)

Famotidine 500 TABLET in 1 BOTTLE (16714-362-05)
(NorthStar RxLLC)

NDC Code16714-362-05
Package Description500 TABLET in 1 BOTTLE (16714-362-05)
Product NDC16714-362
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerNorthStar RxLLC
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/16714-362-05





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