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buspirone hydrochloride

NDC 65841-842, buspirone hydrochloride, tablet, from Zydus Lifesciences Limited.

Product NDC
65841-842
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/65841-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE7.5 mg/1
Package NDCNDC-11Package
65841-842-0165841084201100 TABLET in 1 BOTTLE (65841-842-01)
65841-842-0565841084205500 TABLET in 1 BOTTLE (65841-842-05)
65841-842-10658410842101000 TABLET in 1 BOTTLE (65841-842-10)
65841-842-3065841084230100 BLISTER PACK in 1 CARTON (65841-842-30) / 10 TABLET in 1 BLISTER PACK

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 65841-842 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-842. 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.