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albuterol sulfate

NDC 53489-177, albuterol sulfate, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
53489-177
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/53489-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUTEROL SULFATE4 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
53489-177-0153489017701100 TABLET in 1 BOTTLE (53489-177-01)
53489-177-025348901770250 TABLET in 1 BOTTLE (53489-177-02)
53489-177-0353489017703250 TABLET in 1 BOTTLE (53489-177-03)
53489-177-0553489017705500 TABLET in 1 BOTTLE (53489-177-05)
53489-177-10534890177101000 TABLET in 1 BOTTLE (53489-177-10)

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 53489017701

    GET /v1/drugs/nadac/53489017701

Use it

Look up 53489-177 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53489-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53489-177. 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.