NDC 0093-2210 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-2210

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Teva Pharmaceuticals USA, Inc.
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
0093-2210-01100 TABLET in 1 BOTTLE (0093-2210-01)Nov 11, 1996
0093-2210-05500 TABLET in 1 BOTTLE (0093-2210-05)Nov 11, 1996
0093-2210-9890 TABLET in 1 BOTTLE (0093-2210-98)Jan 12, 2011

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