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Buspirone Hydrochloride

NDC 76420-725, Buspirone Hydrochloride, tablet, from Asclemed USA, Inc..

Product NDC
76420-725
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210907
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-725 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE30 mg/1
Package NDCNDC-11Package
76420-725-0176420072501100 TABLET in 1 BOTTLE, PLASTIC (76420-725-01)
76420-725-0576420072505500 TABLET in 1 BOTTLE, PLASTIC (76420-725-05)
76420-725-307642007253030 TABLET in 1 BOTTLE, PLASTIC (76420-725-30)
76420-725-607642007256060 TABLET in 1 BOTTLE, PLASTIC (76420-725-60)
76420-725-907642007259090 TABLET in 1 BOTTLE, PLASTIC (76420-725-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/97f2d082-0931-4e4f-a5be-7792e399e42b

Use it

Look up 76420-725 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-725 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-725. 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.