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Buspirone Hydrochloride

NDC 70518-4052, Buspirone Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-4052
Status
Listed
Labeler
REMEDYREPACK 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/70518-4052 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUSPIRONE HYDROCHLORIDE15 mg/1
Package NDCNDC-11Package
70518-4052-07051840520030 TABLET in 1 BLISTER PACK (70518-4052-0)
70518-4052-27051840520230 TABLET in 1 BLISTER PACK (70518-4052-2)
70518-4052-37051840520390 TABLET in 1 BOTTLE, PLASTIC (70518-4052-3)
70518-4052-47051840520430 TABLET in 1 BOTTLE, PLASTIC (70518-4052-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fbff8248-b73c-474e-907e-449f8316c629

Use it

Look up 70518-4052 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4052 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4052. 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.