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Zolpidem Tartrate

NDC 71610-254, Zolpidem Tartrate, tablet, film coated, extended release, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-254
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204170
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-254 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLPIDEM TARTRATE12.5 mg/1

Pharmacologic classes

Central Nervous System Depression [PE]; GABA A Agonists [MoA]; Pyridines [CS]; gamma-Aminobutyric Acid-ergic Agonist [EPC]

Package NDCNDC-11Package
71610-254-307161002543030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-254-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ebd6c66b-b230-48d7-b38f-d610b6cb2b6c

Use it

Look up 71610-254 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-254 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-254. 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.