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Sucralfate

NDC 68094-041, Sucralfate oral, suspension, from Precision Dose, Inc..

Product NDC
68094-041
Status
Listed
Labeler
Precision Dose, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68094-041 \
  -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
68094-041-616809400416110 TRAY in 1 CASE (68094-041-61) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)
68094-041-62680940041623 TRAY in 1 CASE (68094-041-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-041-59)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0dc592e9-541c-4fac-8ab5-829d43521c01

Use it

Look up 68094-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68094-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68094-041. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.