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Sucralfate

NDC 68999-106, Sucralfate, suspension, from Chartwell Governmental & Specialty RX, LLC.

Product NDC
68999-106
Status
Listed
Labeler
Chartwell Governmental & Specialty RX, LLC
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211780
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68999-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUCRALFATE1 g/10mL

Pharmacologic classes

Aluminum Complex [EPC]; Organometallic Compounds [CS]

Package NDCNDC-11Package
68999-106-24689990106242 TRAY in 1 BOX (68999-106-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-106-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d1dfbbf2-ea87-41ce-bcc4-bcba99328ed0

Use it

Look up 68999-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68999-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68999-106. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.