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albuterol sulfate

NDC 53489-176, albuterol sulfate, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
53489-176
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072637
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53489-176 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUTEROL SULFATE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
53489-176-0153489017601100 TABLET in 1 BOTTLE (53489-176-01)
53489-176-025348901760250 TABLET in 1 BOTTLE (53489-176-02)
53489-176-0353489017603250 TABLET in 1 BOTTLE (53489-176-03)
53489-176-0553489017605500 TABLET in 1 BOTTLE (53489-176-05)
53489-176-10534890176101000 TABLET in 1 BOTTLE (53489-176-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/87b8cd3c-2849-4b50-b63e-9ea379165c07

  • NADAC price for package 53489017601

    GET /v1/drugs/nadac/53489017601

Use it

Look up 53489-176 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53489-176 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53489-176. 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.