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Zolpidem Tartrate

NDC 72789-390, Zolpidem Tartrate, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-390
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-390 \
  -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
72789-390-217278903902121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-390-21)
72789-390-307278903903030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-390-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/38c838a4-9943-445a-8e80-e823d56eeaa5

Use it

Look up 72789-390 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-390 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-390. 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.