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Buspirone hydrochloride

NDC 77771-237, Buspirone hydrochloride, tablet, from Radha Pharmaceuticals, Inc..

Product NDC
77771-237
Status
Listed
Labeler
Radha Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202087
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/77771-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE15 mg/1
Package NDCNDC-11Package
77771-237-0577771023705500 TABLET in 1 BOTTLE (77771-237-05)
77771-237-607777102376060 TABLET in 1 BOTTLE (77771-237-60)

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 77771-237 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/77771-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 77771-237. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.