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Fluticasone Propionate and Salmeterol DISKUS

NDC 70518-4346, fluticasone propionate and salmeterol, powder, from REMEDYREPACK INC..

Product NDC
70518-4346
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-4346 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUTICASONE PROPIONATE100 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
70518-4346-0705184346001 INHALER in 1 CARTON (70518-4346-0) / 60 POWDER in 1 INHALER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a2d1344-f412-41db-9b54-0c92a0743703

Use it

Look up 70518-4346 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4346 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4346. 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.