NDC 66220-729 – Kristalose

Lactulose 20 g/20g · Powder, For Solution · Oral

Human Prescription Drug

Product NDC66220-729

Product details

Brand name
Kristalose
Generic name
Lactulose
Labeler
Cumberland Pharmaceuticals Inc.
Dosage form
Powder, For Solution
Route
Oral
Marketing category
ANDA · ANDA074712
Marketed since
January 20, 2012
Listing expires
December 31, 2026
Pharmacologic class
Osmotic Laxative

Active ingredients

Uses, dosage, side effects and warnings for Kristalose →

Package NDC codes (1)

Package NDCDescriptionSince
66220-729-3030 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01)Jan 20, 2012

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