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Hyoscyamine Sulfate

NDC 63561-0203, Hyoscyamine Sulfate, tablet, from Granulation Technology, Inc..

Product NDC
63561-0203
Status
Listed
Labeler
Granulation Technology, Inc.
Dosage form
TABLET
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/63561-0203 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYOSCYAMINE SULFATE.125 mg/1
Package NDCNDC-11Package
63561-0203-163561020301100 TABLET in 1 BOTTLE (63561-0203-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/57b12b25-adea-c9bc-e063-6394a90aa925

Use it

Look up 63561-0203 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0203 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63561-0203. 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.