KRISTALOSE
NDC 66220-729 · Cumberland Pharmaceuticals Inc.
Generic namelactulose
Dosage formPOWDER, FOR SOLUTION
RouteORAL
Active ingredient(s)LACTULOSE
Strength20 g/20g
Pharmacologic classAcidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Marketing categoryANDA
Packages
66220-729-30 — 30 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
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, 66220-719 — lactulose, 68999-002 — Lactulose, 68999-004 — Lactulose, 69067-010 — Lactulose, 69067-020 — Lactulose, 73352-900 — Lactulose, 73352-905 — Lactulose, 81033-241 — Lactulose Solution USP, 10 g/15 mL, 82804-107 — Lactulose, 83745-249 — Lactulose, 83745-405 — Lactulose, +14 more