Pramipexole Dihydrochloride
NDC 71335-1537, Pramipexole Dihydrochloride, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-1537
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202633
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1537 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE.125 mg/1
Pharmacologic classes
Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-1537-1 | 71335153701 | 30 TABLET in 1 BOTTLE (71335-1537-1) |
| 71335-1537-2 | 71335153702 | 60 TABLET in 1 BOTTLE (71335-1537-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/468830df-941c-4363-b432-94de9b7fd2ac
Use it
Look up 71335-1537 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1537 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1537. 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.