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Albuterol

NDC 70710-1062, Albuterol, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1062
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
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/70710-1062 \
  -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
70710-1062-170710106201100 TABLET in 1 BOTTLE (70710-1062-1)
70710-1062-570710106205500 TABLET in 1 BOTTLE (70710-1062-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3fa0068-fd12-45de-818e-e929fb45ba05

  • NADAC price for package 70710106201

    GET /v1/drugs/nadac/70710106201

Use it

Look up 70710-1062 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1062 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1062. 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.