Lactulose

Product NDC

35356-754

11-digit product format

353560754

Labeler code

35356

Product ID

35356-754_a836d071-6ac3-45a5-af09-ba587e8c1f2c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lactulose

Dosage form

SOLUTION

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA075993

Marketing category

ANDA

Marketing start

2001-07-26

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