NDC 65162-062 – Sucralfate

Sucralfate 1 g/10mL · Suspension · Oral

Human Prescription Drug

Product NDC65162-062

Product details

Brand name
Sucralfate
Generic name
Sucralfate Oral
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA209356
Marketed since
December 2, 2019
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (2)

Package NDCDescriptionSince
65162-062-05420 mL in 1 BOTTLE (65162-062-05)Dec 2, 2019
65162-062-4810 CUP, UNIT-DOSE in 1 TRAY (65162-062-48) / 10 mL in 1 CUP, UNIT-DOSE (65162-062-47)Dec 2, 2019

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