Hyoscyamine Sulfate
NDC 63561-0197, Hyoscyamine Sulfate, tablet, orally disintegrating, from Granulation Technology, Inc..
- Product NDC
- 63561-0197
- Status
- Listed
- Labeler
- Granulation Technology, Inc.
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0197 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYOSCYAMINE SULFATE.125 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63561-0197-1 | 63561019701 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63561-0197-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4f863ae9-d010-b2f5-e063-6394a90a1a95
Use it
Look up 63561-0197 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0197 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63561-0197. 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.