"31722-063-31" National Drug Code (NDC)

Famotidine 50 mL in 1 BOTTLE (31722-063-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-063-31
Package Description50 mL in 1 BOTTLE (31722-063-31)
Product NDC31722-063
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20230817
Marketing Category NameANDA
Application NumberANDA217330
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/5mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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