NDC 82182-106 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC82182-106

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Pacific Pharma, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019183
Marketed since
February 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
82182-106-14420 mL in 1 BOTTLE (82182-106-14)Feb 1, 2024

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