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Zolpidem Tartrate

NDC 70518-3739, Zolpidem Tartrate, tablet, coated, from REMEDYREPACK INC..

Product NDC
70518-3739
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077322
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3739 \
  -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
70518-3739-07051837390030 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3739-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f8488f3-851d-4111-af23-60f420aad0d6

Use it

Look up 70518-3739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3739. 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.