NDC 82804-102 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-102

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074415
Marketed since
February 17, 2020
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
82804-102-3030 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)May 6, 2024

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