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Hyoscyamine Sulfate ODT

NDC 69367-679, Hyoscyamine Sulfate, tablet, orally disintegrating, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-679
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-679 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYOSCYAMINE SULFATE.125 mg/1
Package NDCNDC-11Package
69367-679-0169367067901100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9429898d-301f-4ebc-8b1d-60595f76f1e3

Use it

Look up 69367-679 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-679 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-679. 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.