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Buspirone Hydrochloride

NDC 70518-2031, Buspirone Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-2031
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204582
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2031 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE10 mg/1
Package NDCNDC-11Package
70518-2031-47051820310460 TABLET in 1 BOTTLE, PLASTIC (70518-2031-4)
70518-2031-57051820310590 TABLET in 1 BOTTLE, PLASTIC (70518-2031-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9fc7091-b3ce-45fd-8d89-aeebdd81c327

Use it

Look up 70518-2031 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2031 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2031. 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.