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"51672-4243-9" National Drug Code (NDC)

Lactulose 1 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLE
(Sun Pharmaceutical Industries, Inc.)

NDC Code51672-4243-9
Package Description1 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLE
Product NDC51672-4243
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20241213
Marketing Category NameANDA
Application NumberANDA218858
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameLACTULOSE
Strength10
Strength Unitg/15mL
Pharmacy ClassesAcidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-4243-9





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