Pramipexole Dihydrochloride
NDC 60687-570, Pramipexole Dihydrochloride, tablet, from American Health Packaging.
- Product NDC
- 60687-570
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090865
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60687-570 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE.25 mg/1
Pharmacologic classes
Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-570-01 | 60687057001 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-570-01) / 1 TABLET in 1 BLISTER PACK (60687-570-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f4d97c2e-f447-4cfe-b9d4-852323f0cfb5NADAC price for package 60687057001
GET /v1/drugs/nadac/60687057001
Use it
Look up 60687-570 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-570 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-570. 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.