Dicyclomine Hydrochloride
NDC 51655-257, Dicyclomine Hydrochloride, tablet, from Northwind Health Company, LLC.
- Product NDC
- 51655-257
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA085223
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-257 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICYCLOMINE HYDROCHLORIDE20 mg/1
Pharmacologic classes
Anticholinergic [EPC]; Cholinergic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51655-257-26 | 51655025726 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-257-26) |
| 51655-257-52 | 51655025752 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-257-52) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c195b8ea-c1bf-453f-e053-2a95a90a2121
Use it
Look up 51655-257 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-257 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-257. 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.