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NDC 24338-026, Amphetamine Sulfate, tablet, from Azurity Pharmaceuticals, Inc..

Product NDC
24338-026
Status
Listed
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200166
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24338-026 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMPHETAMINE SULFATE10 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]

Package NDCNDC-11Package
24338-026-032433800260330 TABLET in 1 BOTTLE (24338-026-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f469fb38-0380-4621-9db3-a4f429126156

Use it

Look up 24338-026 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24338-026 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24338-026. 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.