Primaquine Phosphate
NDC 0024-1596, Primaquine Phosphate, tablet, film coated, from Sanofi-Aventis U.S. LLC.
- Product NDC
- 0024-1596
- Status
- Listed
- Labeler
- Sanofi-Aventis U.S. LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA008316
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0024-1596 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRIMAQUINE PHOSPHATE15 mg/1
Pharmacologic classes
Antimalarial [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0024-1596-01 | 00024159601 | 100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1bfbf4ae-81b8-4160-a00d-6322aadd4b59
Use it
Look up 0024-1596 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0024-1596 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0024-1596. 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.