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Albuterol Sulfate

NDC 70518-3560, albuterol sulfate, solution, from REMEDYREPACK INC..

Product NDC
70518-3560
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
SOLUTION
Route
RESPIRATORY (INHALATION)
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207857
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3560 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUTEROL SULFATE.83 mg/mL

Pharmacologic classes

Adrenergic beta2-Agonists [MoA]; beta2-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
70518-3560-1705183560015 POUCH in 1 CARTON (70518-3560-1) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f9bf2c8-55c0-4b4d-97de-d6c7220c3862

Use it

Look up 70518-3560 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3560 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3560. 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.