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Albuterol Sulfate

NDC 76420-087, Albuterol Sulfate, solution, from Asclemed USA, Inc..

Product NDC
76420-087
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
SOLUTION
Route
RESPIRATORY (INHALATION)
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074880
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUTEROL SULFATE2.5 mg/3mL

Pharmacologic classes

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

Package NDCNDC-11Package
76420-087-03764200087031 VIAL, SINGLE-DOSE in 1 CARTON (76420-087-03) / 3 mL in 1 VIAL, SINGLE-DOSE
76420-087-25764200087251 POUCH in 1 CARTON (76420-087-25) / 25 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=76420-087

Use it

Look up 76420-087 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-087. 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.