NDC 48433-091 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC48433-091

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Safecor Health LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
March 13, 2026
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (1)

Package NDCDescriptionSince
48433-091-20100 BLISTER PACK in 1 CARTON (48433-091-20) / 1 TABLET in 1 BLISTER PACK (48433-091-01)Mar 13, 2026

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