Lactulose

Product NDC

50090-3381

11-digit product format

500903381

Labeler code

50090

Product ID

50090-3381_c0ab7a2b-a02c-4334-9bf6-28fe7cecd08a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lactulose

Dosage form

SOLUTION

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA074602

Marketing category

ANDA

Marketing start

1996-11-14

Marketing end

0000-00-00

Substance

LACTULOSE

Active strength

10 g/15mL

Pharmacologic classes

Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record