LACTULOSE

NDC 0121-1154 · PAI Holdings, LLC dba PAI Pharma

Generic nameLACTULOSE

Dosage formSOLUTION

RouteORAL

Active ingredient(s)LACTULOSE

Strength20 g/30mL

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

Marketing categoryANDA

Packages

0121-1154-00 — 10 TRAY in 1 CASE (0121-1154-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1154-30)

0121-1154-40 — 4 TRAY in 1 CASE (0121-1154-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1154-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0116-4005 — Lactulose, 0121-0873 — Lactulose, 0121-0965 — Lactulose, 0121-1746 — LACTULOSE, 0121-1930 — Lactulose, 0121-4577 — LACTULOSE, 0527-5125 — LACTULOSE, 17856-0874 — Lactulose, 18124-002 — Lactulose, 45963-438 — Lactulose, 45963-439 — Lactulose, 51672-4243 — Lactulose, 55154-9448 — LACTULOSE, 61037-471 — Lactulose Solution USP, 10 g/15 mL, 62135-002 — Lactulose, 62135-003 — Lactulose, 62135-004 — Lactulose, 62135-892 — Lactulose, 63629-8800 — Lactulose, 64980-592 — Lactulose Solution USP, 10 g/15 mL, +14 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.