"67877-843-01" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)
(Ascend Laboratories, LLC)

NDC Code67877-843-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)
Product NDC67877-843
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220708
Marketing Category NameANDA
Application NumberANDA215630
ManufacturerAscend Laboratories, LLC
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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