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Isosorbide dinitrate

NDC 70710-1152, Isosorbide dinitrate, tablet, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1152
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213057
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1152 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ISOSORBIDE DINITRATE40 mg/1

Pharmacologic classes

Nitrate Vasodilator [EPC]; Nitrates [CS]; Vasodilation [PE]

Package NDCNDC-11Package
70710-1152-170710115201100 TABLET in 1 BOTTLE (70710-1152-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16818b32-ee5e-4e07-b848-31e892c4b98a

  • NADAC price for package 70710115201

    GET /v1/drugs/nadac/70710115201

Use it

Look up 70710-1152 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1152 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1152. 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.