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NDC 0024-5401, zolpidem tartrate, tablet, film coated, from Sanofi-Aventis U.S. LLC.

Product NDC
0024-5401
Status
Listed
Labeler
Sanofi-Aventis U.S. LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019908
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0024-5401 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLPIDEM TARTRATE5 mg/1

Pharmacologic classes

Central Nervous System Depression [PE]; GABA A Receptor Positive Modulators [MoA]; gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]

Package NDCNDC-11Package
0024-5401-3100024540131100 TABLET, FILM COATED in 1 BOTTLE (0024-5401-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c36cadf4-65a4-4466-b409-c82020b42452

Use it

Look up 0024-5401 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0024-5401 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0024-5401. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.