NDC 87063-176 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC87063-176

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
ASCLEMED USA INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
November 11, 1996
Listing expires
December 31, 2027
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (6)

Package NDCDescriptionSince
87063-176-01100 TABLET in 1 BOTTLE (87063-176-01)May 18, 2026
87063-176-05500 TABLET in 1 BOTTLE (87063-176-05)May 18, 2026
87063-176-12120 TABLET in 1 BOTTLE (87063-176-12)May 18, 2026
87063-176-3030 TABLET in 1 BOTTLE (87063-176-30)May 18, 2026
87063-176-6060 TABLET in 1 BOTTLE (87063-176-60)May 18, 2026
87063-176-9090 TABLET in 1 BOTTLE (87063-176-90)May 18, 2026

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