Lactulose Solution

NDC 81033-241 · Kesin Pharma Corporation

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameLactulose Solution USP, 10 g/15 mL

Dosage formSOLUTION

RouteORAL, RECTAL

Active ingredient(s)LACTULOSE

Strength10 g/15mL

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

Marketing categoryANDA

Packages

81033-241-50 — 100 CUP, UNIT-DOSE in 1 CASE (81033-241-50) / 15 mL in 1 CUP, UNIT-DOSE (81033-241-15)

81033-241-51 — 100 CUP, UNIT-DOSE in 1 CASE (81033-241-51) / 30 mL in 1 CUP, UNIT-DOSE (81033-241-30)

81033-241-32 — 946 mL in 1 BOTTLE, PLASTIC (81033-241-32)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 66220-719 — lactulose, 66220-729 — lactulose, 68999-002 — Lactulose, 68999-004 — Lactulose, 69067-010 — Lactulose, 69067-020 — Lactulose, 73352-900 — Lactulose, 73352-905 — Lactulose, 82804-107 — Lactulose, 83745-249 — Lactulose, 83745-405 — Lactulose, 85592-819 — lactulose, 85592-829 — lactulose, +14 more

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