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
66689-305_d88c8a64-33d7-4977-9371-2d51c2700589
Product NDC
66689-305
Form
SUSPENSION
Composition / generic term
Sucralfate
Labeler
VistaPharm, LLC
Marketing category
ANDA
Marketing start / end (source format)
20220315
Source listing expiry
20271231

Source-listed ingredients

  • SUCRALFATE — 1 g/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTIC · 66689-305-16

Source and coverage

Open FDA National Drug Code directory

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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