Lactulose Solution

Product NDC

70436-003

11-digit product format

704360003

Labeler code

70436

Product ID

70436-003_6f6e1fd5-b789-489d-a683-bd8b55965ed0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lactulose Solution

Dosage form

SOLUTION

Route

ORAL

Labeler

Slate Run Pharmaceuticals LLC

Application

ANDA209517

Marketing category

ANDA

Marketing start

2019-04-01

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