NDC 52817-840 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC52817-840

Product details

Brand name
Sucralfate
Generic name
Sucralfate Oral
Labeler
TruPharma, LLC
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA213549
Marketed since
April 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (1)

Package NDCDescriptionSince
52817-840-16473 mL in 1 BOTTLE (52817-840-16)Apr 1, 2024

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