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ZOLPIDEM TARTRATE

NDC 72722-103, zolpidem tartrate, tablet, film coated, from The ACME Laboratories Ltd..

Product NDC
72722-103
Status
Listed
Labeler
The ACME Laboratories Ltd.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077214
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72722-103 \
  -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
72722-103-017272201030130 TABLET, FILM COATED in 1 BOTTLE (72722-103-01)
72722-103-0572722010305100 TABLET, FILM COATED in 1 BOTTLE (72722-103-05)
72722-103-07727220103071000 TABLET, FILM COATED in 1 BOTTLE (72722-103-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5679ed64-8424-4e63-a3c9-91d80fff2ca6

Use it

Look up 72722-103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72722-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72722-103. 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.