NDC 51672-4243 – Lactulose

Lactulose 10 g/15mL · Solution · Oral

Human Prescription Drug

Product NDC51672-4243

Product details

Brand name
Lactulose
Generic name
Lactulose
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA218858
Marketed since
June 2, 2025
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
51672-4243-91 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLEJun 2, 2025

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