Buspirone hydrochloride
NDC 77771-234, Buspirone hydrochloride, tablet, from Radha Pharmaceuticals, Inc..
- Product NDC
- 77771-234
- Status
- Listed
- Labeler
- Radha Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202087
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/77771-234 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUSPIRONE HYDROCHLORIDE5 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 77771-234-01 | 77771023401 | 100 TABLET in 1 BOTTLE (77771-234-01) |
| 77771-234-05 | 77771023405 | 500 TABLET in 1 BOTTLE (77771-234-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3f66a3fe-9d73-180c-e063-6394a90aacca
Use it
Look up 77771-234 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/77771-234 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 77771-234. 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.