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Terbutaline Sulfate

NDC 63323-665, TERBUTALINE SULFATE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-665
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076887
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-665 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TERBUTALINE SULFATE1 mg/mL
Package NDCNDC-11Package
63323-665-016332306650125 VIAL, SINGLE-USE in 1 TRAY (63323-665-01) / 1 mL in 1 VIAL, SINGLE-USE (63323-665-00)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cec31032-f366-4524-9e01-63146e473b2b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=63323-665

Use it

Look up 63323-665 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-665 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-665. 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.