"80005-119-16" National Drug Code (NDC)

Famotidine 50 mL in 1 BOTTLE (80005-119-16)
(Carnegie Pharmaceuticals LLC)

NDC Code80005-119-16
Package Description50 mL in 1 BOTTLE (80005-119-16)
Product NDC80005-119
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20230810
Marketing Category NameANDA
Application NumberANDA217137
ManufacturerCarnegie Pharmaceuticals LLC
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/5mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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