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Zolpidem Tartrate

NDC 60687-838, Zolpidem Tartrate, tablet, film coated, from American Health Packaging.

Product NDC
60687-838
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078413
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-838 \
  -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
60687-838-0160687083801100 BLISTER PACK in 1 CARTON (60687-838-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-838-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eb850154-4b4b-4d9a-8476-aea1a93fe8d7

  • NADAC price for package 60687083801

    GET /v1/drugs/nadac/60687083801

Use it

Look up 60687-838 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-838 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-838. 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.