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buspirone hydrochloride

NDC 65841-782, buspirone hydrochloride, tablet, from Zydus Lifesciences Limited.

Product NDC
65841-782
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078888
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE10 mg/1
Package NDCNDC-11Package
65841-782-0165841078201100 TABLET in 1 BOTTLE (65841-782-01)
65841-782-0565841078205500 TABLET in 1 BOTTLE (65841-782-05)
65841-782-10658410782101000 TABLET in 1 BOTTLE (65841-782-10)
65841-782-7765841078277100 BLISTER PACK in 1 CARTON (65841-782-77) / 1 TABLET in 1 BLISTER PACK (65841-782-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1109dd63-6492-49b1-a383-3ab3a80cd6c7

Use it

Look up 65841-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-782. 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.