NDC 62135-436 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-436

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074415
Marketed since
February 17, 2020
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (2)

Package NDCDescriptionSince
62135-436-01100 TABLET in 1 BOTTLE (62135-436-01)Mar 13, 2023
62135-436-9090 TABLET in 1 BOTTLE (62135-436-90)Nov 4, 2022

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