spironolactone
NDC 51655-636, spironolactone, tablet, film coated, from Northwind Health Company, LLC.
- Product NDC
- 51655-636
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205936
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-636 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SPIRONOLACTONE25 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51655-636-26 | 51655063626 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-636-26) |
| 51655-636-52 | 51655063652 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-636-52) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f32e8109-73e1-a249-e053-2995a90a3fae
Use it
Look up 51655-636 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-636 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-636. 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.