"80432-068-35" National Drug Code (NDC)

Lactulose 946 mL in 1 BOTTLE (80432-068-35)
(TriRx Huntsville Pharmaceutical Services)

NDC Code80432-068-35
Package Description946 mL in 1 BOTTLE (80432-068-35)
Product NDC80432-068
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormLIQUID
UsageORAL
Start Marketing Date20241210
Marketing Category NameANDA
Application NumberANDA074623
ManufacturerTriRx Huntsville Pharmaceutical Services
Substance NameLACTULOSE
Strength10
Strength Unitg/15mL
Pharmacy ClassesAcidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

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