"72205-233-84" National Drug Code (NDC)

Famotidine 55 mL in 1 BOTTLE (72205-233-84)
(Novadoz Pharmaceuticals LLC)

NDC Code72205-233-84
Package Description55 mL in 1 BOTTLE (72205-233-84)
Product NDC72205-233
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20250724
Marketing Category NameANDA
Application NumberANDA219863
ManufacturerNovadoz Pharmaceuticals LLC
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/5mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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