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ZOLPIDEM TARTRATE

NDC 71610-915, zolpidem tartrate, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-915
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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/71610-915 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLPIDEM TARTRATE10 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
71610-915-107161009151010 TABLET, FILM COATED in 1 BOTTLE (71610-915-10)
71610-915-147161009151414 TABLET, FILM COATED in 1 BOTTLE (71610-915-14)
71610-915-157161009151515 TABLET, FILM COATED in 1 BOTTLE (71610-915-15)
71610-915-207161009152020 TABLET, FILM COATED in 1 BOTTLE (71610-915-20)
71610-915-217161009152121 TABLET, FILM COATED in 1 BOTTLE (71610-915-21)
71610-915-257161009152525 TABLET, FILM COATED in 1 BOTTLE (71610-915-25)
71610-915-287161009152828 TABLET, FILM COATED in 1 BOTTLE (71610-915-28)
71610-915-307161009153030 TABLET, FILM COATED in 1 BOTTLE (71610-915-30)
71610-915-457161009154545 TABLET, FILM COATED in 1 BOTTLE (71610-915-45)
71610-915-537161009155360 TABLET, FILM COATED in 1 BOTTLE (71610-915-53)
71610-915-597161009155922 TABLET, FILM COATED in 1 BOTTLE (71610-915-59)
71610-915-607161009156090 TABLET, FILM COATED in 1 BOTTLE (71610-915-60)
71610-915-627161009156211 TABLET, FILM COATED in 1 BOTTLE (71610-915-62)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3882d72d-686b-406b-e063-6294a90a0b89

Use it

Look up 71610-915 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-915 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-915. 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.