"72205-145-99" National Drug Code (NDC)

Famotidine 1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)
(Novadoz Pharmaceuticals LLC)

NDC Code72205-145-99
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)
Product NDC72205-145
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240806
Marketing Category NameANDA
Application NumberANDA217400
ManufacturerNovadoz Pharmaceuticals LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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