Lactulose

NDC 62135-003 · Chartwell RX, LLC.

Generic nameLactulose

Dosage formSOLUTION

RouteORAL

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

62135-003-37 — 237 mL in 1 BOTTLE, PLASTIC (62135-003-37)

62135-003-47 — 473 mL in 1 BOTTLE, PLASTIC (62135-003-47)

62135-003-78 — 3785 mL in 1 BOTTLE, PLASTIC (62135-003-78)

62135-003-94 — 946 mL in 1 BOTTLE, PLASTIC (62135-003-94)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 62135-004 — 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, +14 more

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