ZYPITAMAG
NDC 25208-201, Pitavastatin Magnesium, tablet, film coated, from Medicure International Inc.
- Product NDC
- 25208-201
- Status
- Listed
- Labeler
- Medicure International Inc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208379
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/25208-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PITAVASTATIN2 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 25208-201-09 | 25208020109 | 90 TABLET, FILM COATED in 1 BOTTLE (25208-201-09) |
| 25208-201-15 | 25208020115 | 500 TABLET, FILM COATED in 1 BOTTLE (25208-201-15) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c8c50e03-5cb8-43f4-bdef-8edd12f1945f
Use it
Look up 25208-201 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/25208-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 25208-201. 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.