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Triazolam

NDC 70710-1521, Triazolam, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1521
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213003
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1521 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRIAZOLAM.125 mg/1

Pharmacologic classes

Benzodiazepine [EPC]; Benzodiazepines [CS]

Package NDCNDC-11Package
70710-1521-170710152101100 TABLET in 1 BOTTLE (70710-1521-1)
70710-1521-570710152105500 TABLET in 1 BOTTLE (70710-1521-5)
70710-1521-87071015210810 TABLET in 1 BOTTLE (70710-1521-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8d414eb8-eec9-486f-90fc-00eed0cf7daf

  • NADAC price for package 70710152101

    GET /v1/drugs/nadac/70710152101

Use it

Look up 70710-1521 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1521 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1521. 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.