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Albuterol Sulfate

NDC 68084-949, Albuterol Sulfate, tablet, from American Health Packaging.

Product NDC
68084-949
Status
Listed
Labeler
American Health Packaging
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/68084-949 \
  -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
68084-949-256808409492530 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25) / 1 TABLET in 1 BLISTER PACK (68084-949-95)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b0f73459-baeb-42a7-be48-2c3647d9b205

  • NADAC price for package 68084094925

    GET /v1/drugs/nadac/68084094925

Use it

Look up 68084-949 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68084-949 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68084-949. 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.