pramipexole dihydrochloride
NDC 29300-210, pramipexole dihydrochloride, tablet, from Unichem Pharmaceuticals (USA), Inc..
- Product NDC
- 29300-210
- Status
- Listed
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207011
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/29300-210 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRAMIPEXOLE DIHYDROCHLORIDE1 mg/1
Pharmacologic classes
Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 29300-210-10 | 29300021010 | 1000 TABLET in 1 BOTTLE, PLASTIC (29300-210-10) |
| 29300-210-19 | 29300021019 | 90 TABLET in 1 BOTTLE, PLASTIC (29300-210-19) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b978aa75-c62d-444b-9ec6-6c0d21a66688
Use it
Look up 29300-210 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/29300-210 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 29300-210. 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.