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Albuterol

NDC 71205-899, albuterol, tablet, from Proficient Rx LP.

Product NDC
71205-899
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207046
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-899 \
  -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
71205-899-0071205089900100 TABLET in 1 BOTTLE (71205-899-00)
71205-899-11712050899111000 TABLET in 1 BOTTLE (71205-899-11)
71205-899-307120508993030 TABLET in 1 BOTTLE (71205-899-30)
71205-899-5571205089955500 TABLET in 1 BOTTLE (71205-899-55)
71205-899-607120508996060 TABLET in 1 BOTTLE (71205-899-60)
71205-899-907120508999090 TABLET in 1 BOTTLE (71205-899-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/895dff1c-d21c-4470-b021-a5b68364c1ec

Use it

Look up 71205-899 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-899 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-899. 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.