Spironolactone
NDC 0378-0437, spironolactone, tablet, film coated, from Mylan Pharmaceuticals Inc..
- Product NDC
- 0378-0437
- Status
- Listed
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040424
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0437 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SPIRONOLACTONE100 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC]; Aldosterone Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0378-0437-01 | 00378043701 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0437-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/beaf74db-4159-3b59-ef99-575c3ac99aa1NADAC price for package 00378043701
GET /v1/drugs/nadac/00378043701
Use it
Look up 0378-0437 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0437 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0378-0437. 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.