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Terbutaline Sulfate

NDC 71205-939, Terbutaline Sulfate, tablet, from Proficient Rx LP.

Product NDC
71205-939
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211832
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TERBUTALINE SULFATE5 mg/1
Package NDCNDC-11Package
71205-939-0071205093900100 TABLET in 1 BOTTLE (71205-939-00)
71205-939-307120509393030 TABLET in 1 BOTTLE (71205-939-30)
71205-939-5571205093955500 TABLET in 1 BOTTLE (71205-939-55)
71205-939-607120509396060 TABLET in 1 BOTTLE (71205-939-60)
71205-939-907120509399090 TABLET in 1 BOTTLE (71205-939-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a95bc4f-34d3-4b5e-841b-6839e1c1e0c7

Use it

Look up 71205-939 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-939. 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.