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fluticasone propionate and salmeterol

NDC 70518-3968, fluticasone propionate and salmeterol, powder, from REMEDYREPACK INC..

Product NDC
70518-3968
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
POWDER
Route
RESPIRATORY (INHALATION)
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3968 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

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

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3968-0705183968001 POUCH in 1 CARTON (70518-3968-0) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7fecae39-f966-4da5-99f6-4d9428d1b147

Use it

Look up 70518-3968 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3968 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3968. 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.