NDC 17856-0874 – Lactulose

Lactulose 10 g/15mL · Solution · Oral

Human Prescription Drug

Product NDC17856-0874

Product details

Brand name
Lactulose
Generic name
Lactulose
Labeler
Atlantic Biologicals Corp.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA074623
Marketed since
December 3, 2019
Listing expires
December 31, 2026
Pharmacologic class
Osmotic Laxative

Active ingredients

Uses, dosage, side effects and warnings for Lactulose →

Package NDC codes (1)

Package NDCDescriptionSince
17856-0874-350 CUP, UNIT-DOSE in 1 CASE (17856-0874-3) / 30 mL in 1 CUP, UNIT-DOSESep 26, 2025

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