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Albuterol

NDC 70771-1511, Albuterol, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1511
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208884
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1511 \
  -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
70771-1511-170771151101100 TABLET in 1 BOTTLE (70771-1511-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4709eea-e4a2-46e2-850f-1e6afca01893

Use it

Look up 70771-1511 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1511 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1511. 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.