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"18124-001-32" National Drug Code (NDC)

Lactulose 946 mL in 1 BOTTLE (18124-001-32)
(Fresenius Kabi Austria GmbH)

NDC Code18124-001-32
Package Description946 mL in 1 BOTTLE (18124-001-32)
Product NDC18124-001
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20121210
Marketing Category NameANDA
Application NumberANDA090503
ManufacturerFresenius Kabi Austria GmbH
Substance NameLACTULOSE
Strength10
Strength Unitg/15mL
Pharmacy ClassesOsmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/18124-001-32





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