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Fluticasone Propionate and Salmeterol DISKUS

NDC 71205-262, fluticasone propionate and salmeterol, powder, from Proficient Rx LP.

Product NDC
71205-262
Status
Listed
Labeler
Proficient Rx LP
Dosage form
POWDER
Route
RESPIRATORY (INHALATION)
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021077
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-262 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUTICASONE PROPIONATE250 ug/1
  • SALMETEROL XINAFOATE50 ug/1

Pharmacologic classes

Adrenergic beta2-Agonists [MoA]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; beta2-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
71205-262-60712050262601 INHALER in 1 CARTON (71205-262-60) / 60 POWDER in 1 INHALER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6915bd5d-b792-4b1b-8221-7eeb0a8638ba

Use it

Look up 71205-262 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-262 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-262. 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.