United States · FDA National Drug Code directory

Sucralfate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0904-7470_886b2313-1f47-42e6-b0c9-e19e70b59492
Product NDC
0904-7470
Form
SUSPENSION
Composition / generic term
SUCRALFATE Oral Suspension
Labeler
Major Pharmaceuticals
Marketing category
ANDA
Marketing start / end (source format)
20240626
Source listing expiry
20271231

Source-listed ingredients

  • SUCRALFATE — 1 g/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-01
  • 40 CUP, UNIT-DOSE in 1 CASE (0904-7470-18) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-18
  • 20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-56
  • 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-66
  • 100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-72
  • 50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66) · 0904-7470-95

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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