NDC 82804-063 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-063

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
November 11, 1996
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (3)

Package NDCDescriptionSince
82804-063-3030 TABLET in 1 BOTTLE (82804-063-30)Jan 30, 2024
82804-063-6060 TABLET in 1 BOTTLE (82804-063-60)Jan 30, 2024
82804-063-9090 TABLET in 1 BOTTLE (82804-063-90)Jan 30, 2024

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