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Zolpidem Tartrate

NDC 60290-089, Zolpidem Tartrate, capsule, from Umedica Laboratories USA Inc..

Product NDC
60290-089
Status
Listed
Labeler
Umedica Laboratories USA Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA220717
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60290-089 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLPIDEM TARTRATE7.5 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
60290-089-016029000890130 CAPSULE in 1 BOTTLE (60290-089-01)
60290-089-02602900089021000 CAPSULE in 1 BOTTLE (60290-089-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b49f6c18-e155-4728-a79a-9354e8c3c8f4

Use it

Look up 60290-089 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-089 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-089. 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.