"0121-0873-16" National Drug Code (NDC)

Lactulose 473 mL in 1 BOTTLE (0121-0873-16)
(Pharmaceutical Associates, Inc.)

NDC Code0121-0873-16
Package Description473 mL in 1 BOTTLE (0121-0873-16)
Product NDC0121-0873
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20191203
Marketing Category NameANDA
Application NumberANDA074623
ManufacturerPharmaceutical Associates, Inc.
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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